Over-the-counter drug · ANDA
all day pain relief (Naproxen sodium) NDC 0363-0938
Naproxen sodium 200 mg/1 · Tablet, Film coated · Oral · Walgreen Company
NDC codes
FDA NDC DirectoryProduct NDC (as listed)0363-0938Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00363-0938Add the package segment from the table below.
| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0363-0938-82 | 00363093882 | 200 TABLET, FILM COATED in 1 BOTTLE (0363-0938-82)Marketed from Jul 31, 2014 |
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 — 200 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Walgreen CompanyNDC labeler code 0363
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 074661
- Marketing start
- Listing expires
- Other FDA classes
- Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
- Identifiers
- Product ID 0363-0938_020d7f84-045c-47f3-88f9-b153a6d43ab2SPL ID 020d7f84-045c-47f3-88f9-b153a6d43ab2SPL set ID 8ea540bf-4958-41f9-980f-5936c074a51dRxCUI 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
N400363093882followed by a unit qualifier and the quantityPackage 00363-0938-82. 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 0363-0938
- What is NDC 0363-0938?
- 0363-0938 is the product NDC for all day pain relief (naproxen sodium), Naproxen sodium 200 mg/1 tablet, film coated, listed with the FDA by Walgreen Company. It has 1 package NDC, 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?
- Walgreen Company, 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 | 0363-6099 | 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 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 074661
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 |
|---|---|---|---|---|
| All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Walgreen Company | 0363-0368 |
| All Day Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Publix Super Markets Inc | 56062-368 |
| all day reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Publix Super Markets Inc | 56062-490 |
| Basic Care Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Amazon.com Services LLC | 72288-331 |
| basic care naproxen sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Amazon.com Services LLC | 72288-368 |
| Basic Care Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Amazon.com Services LLC | 72288-489 |
| Berkley and Jensen Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | BJWC | 68391-368 |
| betr headache pain reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Live Betr LLC | 80267-001 |
| Care One Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | American Sales Company | 41520-349 |
| Care One Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | American Sales Company | 41520-533 |
| CareOne Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | American Sales Company | 41520-507 |
| DG Health Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Dolgencorp Inc | 55910-481 |
| DG Health Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Dolgencorp Inc | 55910-490 |
| dg health naproxen sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Dolgencorp Inc | 55910-500 |
| dg health naproxen sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Dolgencorp Inc | 55910-729 |
| equaline naproxen sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | United Natural Foods, Inc. dba UNFI | 41163-511 |
| equaline naproxen sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | United Natural Foods, Inc. dba UNFI | 41163-707 |
| exchange select naproxen sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Army & Air Force Exchange Service | 55301-368 |
| foster and thrive all day pain reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Strategic Sourcing Services LLC | 70677-1137 |
| Good Sense Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | L. Perrigo Company | 0113-0901 |
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