Over-the-counter drug · ANDA
Naproxen Sodium NDC 62207-327
Naproxen sodium 220 mg/1 · Tablet · Oral · Granules India Ltd
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 62207-327-41 | 6220703274162207032741 | 24 TABLET in 1 BOTTLE (62207-327-41)Marketed from Jul 16, 2021 | |
| 62207-327-42 | 6220703274262207032742 | 50 TABLET in 1 BOTTLE (62207-327-42)Marketed from Jul 16, 2021 | |
| 62207-327-43 | 6220703274362207032743 | 100 TABLET in 1 BOTTLE (62207-327-43)Marketed from Jul 16, 2021 | |
| 62207-327-47 | 6220703274762207032747 | 500 TABLET in 1 BOTTLE (62207-327-47)Marketed from Jul 16, 2021 | |
| 62207-327-49 | 6220703274962207032749 | 1000 TABLET in 1 BOTTLE (62207-327-49)Marketed from Jul 16, 2021 |
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
- Route
- Oral
- Labeler
- Granules India LtdNDC labeler code 62207
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 091353
- Marketing start
- Listing expires
- Other FDA classes
- Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
- Identifiers
- Product ID 62207-327_f4026a0a-c9cd-3850-e053-2995a90a459cSPL ID f4026a0a-c9cd-3850-e053-2995a90a459cSPL set ID 95ba1722-60ed-4a83-9f26-50c4de8cf180RxCUI 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
N462207032741followed by a unit qualifier and the quantityPackage 62207-0327-41. 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)
USE(S) • 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 62207-327
- What is NDC 62207-327?
- 62207-327 is the product NDC for Naproxen Sodium, Naproxen sodium 220 mg/1 tablet, listed with the FDA by Granules India Ltd. It has 5 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?
- Granules India Ltd, NDC labeler code 62207. 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?
- 144 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 220 mg/1 | Tablet, CoatedOral | AAA Pharmaceutical, Inc. | 57344-244 | 57344-0244-03 |
| 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 | 42507-0245-0142507-0245-0842507-0245-14 |
| 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 | 80425-0531 | 80425-0531-0180425-0531-0280425-0531-03 |
| 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 220 mg/1 | Tablet, CoatedOral | CHAIN DRUG MARKETING ASSOCIATION, INC. | 83324-108 | 83324-0108-0183324-0108-2483324-0108-50 |
Other NDCs under ANDA 091353
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 |
|---|---|---|---|---|
| Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Gobrands, Inc | 82501-1576 |
| All Day Pain Reliefnaproxen sodium tablets, 220 mg | Naproxen sodium 220 mg/1 | TabletOral | HealthLife of USA LLC | 69517-109 |
| Dr Simi All Day Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Farmacias De Similares TX LLC | 85786-104 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | TARGET CORPORATION | 11673-764 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | Safeway, Inc | 21130-061 |
| Naproxen | Naproxen sodium 220 mg/1 | TabletOral | Safeway, Inc | 21130-062 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | Bi-Mart | 37835-594 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | Granules India Ltd | 62207-328 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | CVS | 51316-761 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | CVS | 51316-762 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | Granules India Ltd | 62207-728 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | Granules India Ltd | 62207-729 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coated, Extended releaseOral | SPIRIT PHARMACEUTICALS,LLC | 68210-4096 |
| Rapidol Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Pharmadel LLC | 55758-048 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Granules India Ltd | 62207-761 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Granules India Ltd | 62207-762 |
| Proxen Np 660naproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | OPMX LLC | 69729-123 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | Granules USA, Inc. | 69848-010 |