Over-the-counter drug · ANDA
All Day Pain Relief NDC 69517-109
naproxen sodium tablets, 220 mg · Naproxen sodium 220 mg/1 · Tablet · Oral · HealthLife of USA LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 69517-109-02 | 69517010902 | 2 POUCH in 1 POUCH (69517-109-02) / 2 TABLET in 1 POUCHMarketed from Apr 7, 2016 | |
| 69517-109-04 | 69517010904 | 400 BOTTLE in 1 BOTTLE (69517-109-04) / 100 BOTTLE in 1 BOTTLE (69517-109-01) / 24 CARTON in 1 BOTTLE (69517-109-24) / 1 TABLET in 1 CARTONMarketed from Apr 7, 2016 | |
| 69517-109-25 | 69517010925 | 25 POUCH in 1 BOX (69517-109-25) / 2 TABLET in 1 POUCHMarketed from Apr 7, 2016 | |
| 69517-109-50 | 69517010950 | 50 POUCH in 1 BOX (69517-109-50) / 2 TABLET in 1 POUCHMarketed from Apr 7, 2016 |
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 tablets, 220 mg
- Active ingredients
- Naproxen sodium — 220 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- HealthLife of USA LLC
- 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 69517-109_046b91ed-d78b-42c0-b822-77fcbdeff84bSPL ID 046b91ed-d78b-42c0-b822-77fcbdeff84bSPL set ID 7b0cb91e-5465-40ef-9f82-919f7d984f17RxCUI 849574UNII 9TN87S3A3CUPC 0069517109248
- 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
N469517010902followed by a unit qualifier and the quantityPackage 69517-0109-02. 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 ■ headache ■ menstrual cramps ■ toothache ■ the common cold ■ temporarily reduces fever
Excerpt only. Read the full label for complete information.
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 |
|---|---|---|---|---|
| Rapidol Naproxennaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, CoatedOral | Pharmadel LLC | 55758-048 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | Granules India Ltd | 62207-728 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coated, Extended releaseOral | SPIRIT PHARMACEUTICALS,LLC | 68210-4096 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | Granules India Ltd | 62207-327 |
| 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 | TARGET CORPORATION | 11673-764 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Granules India Ltd | 62207-762 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Granules India Ltd | 62207-761 |
| Pain Reliefnaproxen sodium | Naproxen sodium 220 mg/1 | Tablet, Film coatedOral | Gobrands, Inc | 82501-1576 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | Bi-Mart | 37835-594 |
| Naproxen | Naproxen sodium 220 mg/1 | TabletOral | Safeway, Inc | 21130-062 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | Safeway, Inc | 21130-061 |
| 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 | Granules India Ltd | 62207-729 |
| Naproxen Sodium | Naproxen sodium 220 mg/1 | TabletOral | Granules USA, Inc. | 69848-010 |
| Proxen Np 660naproxen sodium | Naproxen sodium 220 mg/1 | TabletOral | OPMX LLC | 69729-123 |