Over-the-counter drug · ANDA
naproxen sodium NDC 37808-713
Naproxen sodium 220 mg/1 · Tablet, Film coated · Oral · H E B
NDC codes
FDA NDC DirectoryProduct NDC (as listed)37808-713Labeler and product segments. Claims need a package NDC.
Product NDC at billing width37808-0713Add the package segment from the table below.
| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 37808-713-62 | 37808071362 | 1 BOTTLE in 1 CARTON (37808-713-62) / 24 TABLET, FILM COATED in 1 BOTTLE (37808-713-24)Marketed from Jun 19, 2026 | |
| 37808-713-71 | 37808071371 | 1 BOTTLE in 1 CARTON (37808-713-71) / 50 TABLET, FILM COATED in 1 BOTTLE (37808-713-50)Marketed from Jun 19, 2026 | |
| 37808-713-75 | 37808071375 | 1 BOTTLE in 1 CARTON (37808-713-75) / 90 TABLET, FILM COATED in 1 BOTTLE (37808-713-90)Marketed from Jun 19, 2026 | |
| 37808-713-79 | 37808071379 | 400 TABLET, FILM COATED in 1 BOTTLE (37808-713-79)Marketed from Oct 3, 2017 |
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)
- naproxen sodium
- Generic name (nonproprietary)
- naproxen sodium
- Active ingredients
- Naproxen sodium — 220 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- H E BNDC labeler code 37808
- 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 37808-713_c6dc355a-939a-4205-80cc-20b92d623ebaSPL ID c6dc355a-939a-4205-80cc-20b92d623ebaSPL set ID b5dcf3df-2628-49c7-9d96-64886bebe631RxCUI 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
N437808071362followed by a unit qualifier and the quantityPackage 37808-0713-62. 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 37808-713
- What is NDC 37808-713?
- 37808-713 is the product NDC for naproxen sodium, Naproxen sodium 220 mg/1 tablet, film coated, listed with the FDA by H E B. It has 4 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- naproxen sodium.
- What is the active ingredient?
- Naproxen sodium.
- Who is the labeler?
- H E B, NDC labeler code 37808. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for naproxen sodium?
- 145 other product NDCs are listed under this name. See all naproxen sodium NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other naproxen sodium products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| naproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Amazon.com Services LLC | 72288-988 | 72288-0988-75 |
| Naproxen Sodium | Naproxen sodium 550 mg/1 | TabletOral | Advanced Rx of Tennessee, LLC | 80425-0574 | 80425-0574-0180425-0574-0280425-0574-03 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | HYVEE INC | 42507-245 | 42507-0245-0142507-0245-14 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | HYVEE INC | 42507-844 | 42507-0844-0142507-0844-14 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Capsule, Liquid filledOral | TARGET Corporation | 11673-651 | 11673-0651-78 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Safeway | 21130-593 | 21130-0593-79 |
| Naproxen Sodium | Naproxen sodium 550 mg/1 | TabletOral | Advanced Rx of Tennessee, LLC | 80425-0532 | 80425-0532-0180425-0532-0280425-0532-03 |
| Naproxen Sodium | Naproxen sodium 550 mg/1 | TabletOral | Advanced Rx of Tennessee, LLC | 80425-0531 | 80425-0531-0180425-0531-0280425-0531-03 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | CHAIN DRUG MARKETING ASSOCIATION, INC. | 83324-108 | 83324-0108-0183324-0108-2483324-0108-50 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | CHAIN DRUG MARKETING ASSOCIATION, INC. | 83324-109 | 83324-0109-0183324-0109-50 |
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 |
| naproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | H E B | 37808-652 |
| Leader All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Cardinal Health 110, LLC. dba Leader | 70000-0201 |
| Rugby All Day Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Rugby Laboratories | 0536-1093 |
| all day pain reliefnaproxen sodium | Naproxen sodium 200 mg/1 | Tablet, Film coatedOral | Walgreen Company | 0363-0938 |
| signature care naproxen sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Safeway | 21130-180 |
| all day reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Publix Super Markets Inc | 56062-490 |
| rugby all day reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Rugby Laboratories | 0536-1094 |
| Basic Care Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Amazon.com Services LLC | 72288-331 |
| Rugby All Day Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-3009 |
| naproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Amazon.com Services LLC | 72288-988 |
| basic care naproxen sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Amazon.com Services LLC | 72288-368 |
| equaline naproxen sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | United Natural Foods, Inc. dba UNFI | 41163-707 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Meijer Distribution Inc | 41250-477 |
| naproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | CVS Pharmacy | 59779-914 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Padagis Israel Pharmaceuticals Ltd | 45802-490 |
| up and up naproxen sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Target Corporation | 11673-368 |
| Berkley and Jensen Naproxen Sodiumnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | BJWC | 68391-368 |
| TopCare All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Topco Associates LLC | 36800-368 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 63187-596 |
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