Over-the-counter drug · ANDA
All Day Pain Relief (Naproxen sodium) NDC 0363-6099
Naproxen sodium 220 mg/1 · Tablet, Coated · Oral · WALGREENS
NDC codes
FDA NDC DirectoryProduct NDC (as listed)0363-6099Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00363-6099Add the package segment from the table below.
| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0363-6099-01 | 0036360990100363609901 | 100 TABLET, COATED in 1 BOTTLE (0363-6099-01)Marketed from Jul 8, 2019 | |
| 0363-6099-05 | 0036360990500363609905 | 50 TABLET, COATED in 1 BOTTLE (0363-6099-05)Marketed from Jul 8, 2019 | |
| 0363-6099-20 | 0036360992000363609920 | 200 TABLET, COATED in 1 BOTTLE (0363-6099-20)Marketed from Jul 8, 2019 |
How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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, Coated
- Route
- Oral
- Labeler
- WALGREENSNDC labeler code 0363
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 090545
- Marketing start
- Listing expires
- Other FDA classes
- Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
- Identifiers
- Product ID 0363-6099_13b172b6-b829-8fe5-e063-6294a90a37e3SPL ID 13b172b6-b829-8fe5-e063-6294a90a37e3SPL set ID 8771300f-e907-3d53-e053-2a95a90ae402RxCUI 849574UNII 9TN87S3A3C
- 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
N400363609901followed by a unit qualifier and the quantityPackage 00363-6099-01. 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)
temporarily relieves minor aches and pain due to: minor pain of arthritis muscular aches backache menstrual cramps headache toothache the common cold temporarily reduces fever
Excerpt only. Read the full label for complete information.
About NDC 0363-6099
- What is NDC 0363-6099?
- 0363-6099 is the product NDC for All Day Pain Relief (naproxen sodium), Naproxen sodium 220 mg/1 tablet, coated, listed with the FDA by WALGREENS. It has 3 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?
- WALGREENS, NDC labeler code 0363. 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, Film coatedOral | WALMART INC. | 79903-005 | 79903-0005-2079903-0005-2579903-0005-27+1 more |
| 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 090545
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 |
|---|---|---|---|---|
| Naproxen Sodium 220mg | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Grocery Outlet | 85828-394 |
| Naproxen Sodiumnaproxen sodium, coated tablets | Naproxen sodium 220 mg/1 | TabletOral | MARKSANS PHARMA LIMITED | 25000-141 |
| Naproxen Sodiumnaproxen sodium tablet, coated | Naproxen sodium 220 mg/1 | TabletOral | MARKSANS PHARMA LIMITED | 25000-144 |
| Calmadol Pain Relievernaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | GRANDALL DISTRIBUTING, LLC | 48201-007 |
| Naproxen Caplets All day relief for painnaproxen sodium 220 mg | Naproxen sodium 220 mg/1 | TabletOral | Allegiant Health | 69168-362 |
| Flanax Pain Reliever/Fever Reducernaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Navajo Manufacturing Company Inc. | 67751-125 |
| Naproxen Sodium 220mg | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Allegiant Health | 69168-395 |
| Naproxen Capletsnaproxen sodium 220 mg | Naproxen sodium 220 mg/1 | TabletOral | Allegiant Health | 69168-394 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Kroger Company | 41226-609 |
| Flanax Pain Reliever/Fever reducernaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Belmora LLC | 27854-505 |
| Belmora Flanaxnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Belmora LLC | 27854-555 |
| All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | Walmart Inc. | 79903-389 |
| Naproxen Sodium 220mg | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Command Brands, LLC | 69197-394 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | TIME CAP LABORATORIES, INC | 49483-608 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | TIME CAP LABORATORIES, INC | 49483-609 |
| All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | WALGREENS | 0363-9608 |
| Back And Muscle Painnaproxen | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | WALGREENS | 0363-9609 |
| Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | BETTER LIVING BRANDS, LLC | 21130-608 |
| All Day Back and Muscle Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Walmart Inc. | 79903-609 |
| Naproxen Sodium 220mg | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Athlete's Needs, Inc. | 53185-394 |
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