Over-the-counter drug · OTC MONOGRAPH DRUG
TYLENOL Extra Strength (Acetaminophen) NDC 50580-449
Acetaminophen 500 mg/1 · Tablet, Film coated · Oral · Kenvue Brands LLC
NDC codes
FDA NDC DirectoryProduct NDC (as listed)50580-449Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50580-0449Add the package segment from the table below.
| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 50580-449-00 | 5058004490050580044900 | 1 BOTTLE, PLASTIC in 1 CARTON (50580-449-00) / 125 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Aug 19, 1984 | |
| 50580-449-05 | 5058004490550580044905 | 1 BOTTLE, PLASTIC in 1 CARTON (50580-449-05) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Aug 19, 1984 | |
| 50580-449-08 | 5058004490850580044908 | 2 TABLET, FILM COATED in 1 POUCH (50580-449-08)Marketed from Aug 19, 1984 | |
| 50580-449-09 | 5058004490950580044909 | 1 BOTTLE, PLASTIC in 1 CARTON (50580-449-09) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Aug 19, 1984 | |
| 50580-449-10 | 5058004491050580044910 | 50 POUCH in 1 TRAY (50580-449-10) / 2 TABLET, FILM COATED in 1 POUCHMarketed from Aug 19, 1984 | |
| 50580-449-11 | 5058004491150580044911 | 50 POUCH in 1 TRAY (50580-449-11) / 2 TABLET, FILM COATED in 1 POUCHMarketed from Aug 19, 1984 | |
| 50580-449-12 | 5058004491250580044912 | 12 VIAL, PLASTIC in 1 PACKAGE (50580-449-12) / 10 TABLET, FILM COATED in 1 VIAL, PLASTICMarketed from Oct 21, 2014 | |
| 50580-449-13 | 5058004491350580044913 | 3 POUCH in 1 CARTON (50580-449-13) / 2 TABLET, FILM COATED in 1 POUCHMarketed from Aug 19, 1984 | |
| 50580-449-14 | 5058004491450580044914 | 2 TABLET, FILM COATED in 1 POUCH (50580-449-14)Marketed from Aug 19, 1984 | |
| 50580-449-15 | 5058004491550580044915 | 10 TABLET, FILM COATED in 1 VIAL, PLASTIC (50580-449-15)Marketed from Aug 19, 1984 | |
| 50580-449-23 | 5058004492350580044923 | 1 BOTTLE, PLASTIC in 1 CARTON (50580-449-23) / 150 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Aug 19, 1984 | |
| 50580-449-31 | 5058004493150580044931 | 1 BOTTLE, PLASTIC in 1 CARTON (50580-449-31) / 36 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Aug 19, 1984 | |
| 50580-449-34 | 5058004493450580044934 | 325 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50580-449-34)Marketed from Aug 19, 1984 | |
| 50580-449-35 | 5058004493550580044935 | 1 BOTTLE, PLASTIC in 1 CARTON (50580-449-35) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Aug 19, 1984 | |
| 50580-449-36 | 5058004493650580044936 | 1 BOTTLE, PLASTIC in 1 CARTON (50580-449-36) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Aug 19, 1984 | |
| 50580-449-37 | 5058004493750580044937 | 320 TABLET, FILM COATED in 1 BOTTLE (50580-449-37)Marketed from Mar 31, 2026 | |
| 50580-449-61 | 5058004496150580044961 | 1 BOTTLE, PLASTIC in 1 CARTON (50580-449-61) / 225 TABLET, FILM COATED in 1 BOTTLE, PLASTICMarketed from Aug 19, 1984 | |
| 50580-449-62 | 5058004496250580044962 | 325 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50580-449-62)Marketed from Aug 19, 1984 | |
| 50580-449-66 | 5058004496650580044966 | 2 BOTTLE in 1 CARTON (50580-449-66) / 100 TABLET, FILM COATED in 1 BOTTLEMarketed from May 1, 2024 | |
| 50580-449-84 | 5058004498450580044984 | 2 TABLET, FILM COATED in 1 POUCH (50580-449-84)Marketed from Aug 19, 1984 | |
| 50580-449-85 | 5058004498550580044985 | 50 POUCH in 1 TRAY (50580-449-85) / 2 TABLET, FILM COATED in 1 POUCHMarketed from Aug 19, 1984 | |
| 50580-449-86 | 5058004498650580044986 | 50 POUCH in 1 TRAY (50580-449-86) / 2 TABLET, FILM COATED in 1 POUCHMarketed from Aug 19, 1984 | |
| 50580-449-87 | 5058004498750580044987 | 3 POUCH in 1 CARTON (50580-449-87) / 2 TABLET, FILM COATED in 1 POUCHMarketed from Aug 19, 1984 | |
| 50580-449-96 | 5058004499650580044996 | 1 BOTTLE in 1 CARTON (50580-449-96) / 50 TABLET, FILM COATED in 1 BOTTLEMarketed from Jun 25, 2018 | |
| 50580-449-97 | 5058004499750580044997 | 249 TABLET, FILM COATED in 1 PACKAGE, COMBINATION (50580-449-97)Marketed from Jan 28, 2019 | |
| 50580-449-98 | 5058004499850580044998 | 110 TABLET, FILM COATED in 1 PACKAGE, COMBINATION (50580-449-98)Marketed from Jan 28, 2019 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- TYLENOL Extra Strength
- Generic name (nonproprietary)
- acetaminophen
- Active ingredients
- Acetaminophen — 500 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Kenvue Brands LLCNDC labeler code 50580
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication M 013
- Marketing start
- Listing expires
- Identifiers
- Product ID 50580-449_5448d8a1-99d5-a698-e063-6294a90aff9bSPL ID 5448d8a1-99d5-a698-e063-6294a90aff9bSPL set ID 59773893-09a8-47a2-943a-e9ea9da4458aRxCUI 198440, 209459UNII 362O9ITL9DUPC 0300450449108
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N450580044900followed by a unit qualifier and the quantityPackage 50580-0449-00. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Uses temporarily relieves minor aches and pains due to: the common cold headache backache minor pain of arthritis toothache muscular aches premenstrual and menstrual cramps temporarily reduces fever
Excerpt only. Read the full label for complete information.
About NDC 50580-449
- What is NDC 50580-449?
- 50580-449 is the product NDC for TYLENOL Extra Strength (acetaminophen), Acetaminophen 500 mg/1 tablet, film coated, listed with the FDA by Kenvue Brands LLC. It has 26 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- TYLENOL Extra Strength (Acetaminophen).
- What is the active ingredient?
- Acetaminophen.
- Who is the labeler?
- Kenvue Brands LLC, NDC labeler code 50580. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for TYLENOL Extra Strength?
- 23 other product NDCs are listed under this name. See all TYLENOL Extra Strength NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other TYLENOL Extra Strength products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| TYLENOL Extra Strengthacetaminophen | Acetaminophen 960 mg/30mL | SuspensionOral | Kenvue Brands LLC | 50580-187 | 50580-0187-08 |
| TYLENOL Extra Strengthacetaminophen | Acetaminophen 500 mg/1 | Capsule, Liquid filledOral | Kenvue Brands LLC | 50580-469 | 50580-0469-1850580-0469-4050580-0469-75 |
| TYLENOL Extra Strengthacetaminophen | Acetaminophen 500 mg/1 | Tablet, Film coatedOral | Kenvue Brands LLC | 50580-108 | 50580-0108-25 |
| TYLENOL Extra Strengthacetaminophen | Acetaminophen 500 mg/1 | Tablet, Film coatedOral | Kenvue Brands LLC | 50580-491 | 50580-0491-0150580-0491-1050580-0491-70 |
| Tylenol Extra Strengthacetaminophen | Acetaminophen 500 mg/1 | Tablet, Film coatedOral | Kenvue Brands LLC | 50580-472 | 50580-0472-0150580-0472-0250580-0472-03+1 more |
| Tylenol Extra Strengthacetaminophen | Acetaminophen 500 mg/1 | TabletOral | R J General Corporation | 70264-027 | 70264-0027-01 |
| TYLENOL Extra Strengthacetaminophen | Acetaminophen 500 mg/1 | Tablet, CoatedOral | Kenvue Brands LLC | 50580-490 | 50580-0490-0250580-0490-1050580-0490-20+4 more |
| TYLENOL Extra Strengthacetaminophen | Acetaminophen 500 mg/1 | Tablet, Film coatedOral | Kenvue Brands LLC | 50580-457 | 50580-0457-1050580-0457-1150580-0457-70 |
| TYLENOL Extra Strengthacetaminophen | Acetaminophen 500 mg/.95g | PowderOral | Kenvue Brands LLC | 50580-209 | 50580-0209-0250580-0209-04 |
| Tylenol Extra Strengthacetaminophen | Acetaminophen 500 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-5469 | 50090-5469-00 |
Other NDCs under M 013
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Childrens Acetaminophenacetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | Grocery Outlet, Inc. | 85828-922 |
| Pain Relief Regular Strengthacetaminophen | Acetaminophen 325 mg/1 | TabletOral | CHAIN DRUG MARKETING ASSOCIATION INC | 83324-076 |
| equate pain and fever childrensacetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | Wal-Mart Stores Inc | 49035-042 |
| good neighbor pharmacy childrens pain and feveracetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | Amerisource Bergen | 46122-210 |
| Aspirin | Aspirin 81 mg/1 | Tablet, Delayed releaseOral | GOODSENSE | 50804-880 |
| Tylenol PM Extra Strengthacetaminophen and diphenhydramine hydrochloride | Acetaminophen 500 mg/1; Diphenhydramine hydrochloride 25 mg/1 | Tablet, Film coatedOral | Morning Star OTC | 53209-1002 |
| Acetaminophen | Acetaminophen 500 mg/1 | TabletOral | Cardinal Health 107, LLC | 55154-7897 |
| Headache Formula Extra Strengthacetaminophen, aspirin, caffeine | Acetaminophen 250 mg/1 + 2 more ingredients | Tablet, Film coatedOral | ARMY AND AIR FORCE EXCHANGE SERVICE | 55301-334 |
| childrens pain and feveracetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | Walgreen Company | 0363-1239 |
| Tylenol PMacetaminophen, diphenhydramine hydrochloride | Acetaminophen 500 mg/1; Diphenhydramine hydrochloride 25 mg/1 | Tablet, Film coatedOral | Savings Distributors LLC | 73097-013 |
| Alka-Seltzer Originalanhydrous citric acid, aspirin, and sodium bicarbonate | Anhydrous citric acid 1000 mg/1 + 2 more ingredients | Tablet, EffervescentOral | Bayer HealthCare LLC. | 0280-4000 |
| Aspirin Low Doseaspirin | Aspirin 81 mg/1 | Tablet, Delayed releaseOral | Strategic Sourcing Services LLC | 70677-1260 |
| basic care infants pain and feveracetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | Amazon.com Services LLC | 72288-946 |
| Acetaminophen | Acetaminophen 500 mg/1 | TabletOral | Sportpharm LLC | 85766-223 |
| Pain Relief Aspirin Low Doseaspirin | Aspirin 81 mg/1 | Tablet, Delayed releaseOral | Rite Aid Corporation | 11822-0600 |
| Equaline Effervescent Antacid and Pain Reliefaspirin, citric acid, sodium bicarbonate | Aspirin 325 mg/1 + 2 more ingredients | Tablet, EffervescentOral | United Natural Foods, Inc. dba UNFI | 41163-421 |
| Night Time Severe Cold and Cough Reliefacetaminophen, diphenhydramine hcl, phenylephrine hcl | Acetaminophen 325 mg/15mL + 2 more ingredients | LiquidOral | Chain Drug Consortium, LLC | 68016-154 |
| Tension Headache Relief | Acetaminophen 500 mg/1; Caffeine 65 mg/1 | Capsule, CoatedOral | Allegiant Health | 69168-001 |
| Childrens Acetaminophenacetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | Proficient Rx LP | 71205-263 |
| Chewable Aspirinaspirin | Aspirin 81 mg/1 | Tablet, ChewableOral | Chain Drug Marketing Association, Inc. | 83324-075 |
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