Over-the-counter drug · ANDA
All Day Pain Relief (Naproxen sodium) NDC 79903-005
Naproxen sodium 220 mg/1 · Tablet, Film coated · Oral · WALMART INC.
NDC codes
FDA NDC DirectoryProduct NDC (as listed)79903-005Labeler and product segments. Claims need a package NDC.
Product NDC at billing width79903-0005Add the package segment from the table below.
| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 79903-005-20 | 7990300052079903000520 | 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-20)Marketed from Oct 22, 2020 | |
| 79903-005-25 | 7990300052579903000525 | 225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-25)Marketed from Oct 22, 2020 | |
| 79903-005-27 | 7990300052779903000527 | 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-27)Marketed from Oct 22, 2020 | |
| 79903-005-90 | 7990300059079903000590 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-90)Marketed from Oct 22, 2020 |
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)
- All Day Pain Relief
- Generic name (nonproprietary)
- naproxen sodium
- Active ingredients
- Naproxen sodium — 220 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- WALMART INC.NDC labeler code 79903
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 204872
- Marketing start
- Listing expires
- Other FDA classes
- Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
- Identifiers
- Product ID 79903-005_7ff7ea22-53e8-4895-9960-c48a4bc4ad83SPL ID 7ff7ea22-53e8-4895-9960-c48a4bc4ad83SPL set ID c4909e43-57ba-44bc-a234-a02cc884891cRxCUI 849574UNII 9TN87S3A3CUPC 0194346189120
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
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
N479903000520followed by a unit qualifier and the quantityPackage 79903-0005-20. 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: headache muscular aches the common cold toothache menstrual cramps backache minor pain of arthritis temporarily reduces fever
Excerpt only. Read the full label for complete information.
About NDC 79903-005
- What is NDC 79903-005?
- 79903-005 is the product NDC for All Day Pain Relief (naproxen sodium), Naproxen sodium 220 mg/1 tablet, film coated, listed with the FDA by WALMART INC.. It has 4 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- All Day Pain Relief (Naproxen Sodium).
- What is the active ingredient?
- Naproxen sodium.
- Who is the labeler?
- WALMART INC., NDC labeler code 79903. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for All Day Pain Relief?
- 9 other product NDCs are listed under this name. See all All Day Pain Relief NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other All Day Pain Relief products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Walmart Inc. | 79903-389 | 79903-0389-50 |
| All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | WALGREENS | 0363-6099 | 00363-6099-0100363-6099-0500363-6099-20 |
| All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | WALGREENS | 0363-9608 | 00363-9608-0500363-9608-0900363-9608-20+4 more |
| All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | H E B | 37808-068 | 37808-0068-2437808-0068-50 |
| all day pain reliefnaproxen sodium | Naproxen sodium 200 mg/1 | Tablet, Film coatedOral | Walgreen Company | 0363-0938 | 00363-0938-82 |
| All Day Pain Reliefnaproxen sodium tablets, 220 mg | Naproxen sodium 220 mg/1 | TabletOral | HealthLife of USA LLC | 69517-109 | 69517-0109-0269517-0109-0469517-0109-25+1 more |
| All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | VALU MERCHANDISERS COMPANY | 63941-144 | 63941-0144-0163941-0144-0263941-0144-03 |
| All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | VALU MERCHANDISERS COMPANY | 63941-245 | 63941-0245-0163941-0245-0263941-0245-03 |
| All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Walgreen Company | 0363-0368 | 00363-0368-7100363-0368-7500363-0368-76 |
Other NDCs under ANDA 204872
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 |
|---|---|---|---|---|
| 24/7 Life by 7-Eleven Naproxen Sodiumnaproxen sodium tablet, film coated | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Lil' Drug Store Products, Inc. | 66715-5428 |
| AnaDentnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Belmora LLC | 27854-170 |
| Artridolnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Zapotol Products Corp | 59428-604 |
| Back and Muscle Painnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Rite Aid Corporation | 11822-4170 |
| Back and Muscle Painnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 51316-817 |
| First Aid Direct All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Cintas Corporation | 42961-122 |
| Flanaxnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Belmora LLC | 27854-160 |
| Flanax Menstrual Pain Relievernaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Belmora LLC | 27854-165 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Better Living Brands, LLC | 21130-674 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Amerisource Bergen | 46122-562 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Amerisource Bergen | 46122-564 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | L.N.K. International, Inc. | 50844-261 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Family Dollar Services Inc | 55319-406 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Family Dollar Services Inc | 55319-717 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Geri-Care Pharmaceutical Corp | 57896-954 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | NuCare Pharmaceuticals,Inc. | 68071-5039 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Preferred Pharmaceuticals, Inc. | 68788-7572 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Proficient Rx LP | 71205-595 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-1282 |
| Naproxen Back and Muscle Painnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | L.N.K. International, Inc. | 50844-714 |
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