Over-the-counter drug · ANDA
All Day Pain Relief (Naproxen sodium) NDC 63941-245
Naproxen sodium 220 mg/1 · Tablet, Coated · Oral · VALU MERCHANDISERS COMPANY
NDC codes
FDA NDC DirectoryProduct NDC (as listed)63941-245Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63941-0245Add the package segment from the table below.
| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 63941-245-01 | 6394102450163941024501 | 1 BOTTLE, PLASTIC in 1 CARTON (63941-245-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTICMarketed from Jun 10, 2010 | |
| 63941-245-02 | 6394102450263941024502 | 1 BOTTLE, PLASTIC in 1 CARTON (63941-245-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTICMarketed from May 19, 2010 | |
| 63941-245-03 | 6394102450363941024503 | 1 BOTTLE, PLASTIC in 1 CARTON (63941-245-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTICMarketed from May 19, 2010 |
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, Coated
- Route
- Oral
- Labeler
- VALU MERCHANDISERS COMPANYNDC labeler code 63941
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 079096
- Marketing start
- Marketing end
- Other FDA classes
- Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
- Identifiers
- Product ID 63941-245_28729f2d-cd7e-c174-e063-6394a90ac876SPL ID 28729f2d-cd7e-c174-e063-6394a90ac876SPL set ID 593b915f-045a-40b7-b86e-0d1cb41f2bb8RxCUI 849574UNII 9TN87S3A3CUPC 0070038577805
- 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
N463941024501followed by a unit qualifier and the quantityPackage 63941-0245-01. 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)
Uses temporarily relieves minor aches and pains 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 63941-245
- What is NDC 63941-245?
- 63941-245 is the product NDC for All Day Pain Relief (naproxen sodium), Naproxen sodium 220 mg/1 tablet, coated, listed with the FDA by VALU MERCHANDISERS COMPANY. 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?
- VALU MERCHANDISERS COMPANY, NDC labeler code 63941. 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 | 0363-6099 | 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, Film coatedOral | Walgreen Company | 0363-0368 | 00363-0368-7100363-0368-7500363-0368-76 |
Other NDCs under ANDA 079096
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 | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | AAA Pharmaceutical, Inc. | 57344-145 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | AAA Pharmaceutical, Inc. | 57344-244 |
| Medique Mediproxennaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Unifirst First Aid Corporation | 47682-237 |
| All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | H E B | 37808-068 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | WinCo Foods, LLC | 67091-138 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | WinCo Foods, LLC | 67091-140 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | CHAIN DRUG MARKETING ASSOCIATION, INC. | 83324-108 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | CHAIN DRUG MARKETING ASSOCIATION, INC. | 83324-109 |
| Medique Mediproxennaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-2388 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | HYVEE INC | 42507-245 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | FSA STORE INC. | 81522-045 |
| CAREALL Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | New World Imports, Inc. | 51824-072 |
| Medique at Home Mediproxennaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Unifirst First Aid Corporation | 47682-737 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Chain Drug Marketing Association | 63868-465 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Chain Drug Marketing Association | 63868-466 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | DISCOUNT DRUG MART | 53943-144 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | AMERIFOODS TRADING COMPANY | 61504-145 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | VALU MERCHANDISERS COMPANY | 63941-444 |
| Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | DISCOUNT DRUG MART | 53943-145 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | VALU MERCHANDISERS COMPANY | 63941-445 |
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