back and muscle pain
- Product NDC
- 11822-1330
- 11-digit product format
- 118221330
- Labeler code
- 11822
- Product ID
- 11822-1330_13a016c8-9c54-469b-bce7-336a89fa48fc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA074661
- Marketing category
- ANDA
- Marketing start
- 2019-06-06
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-1330-1 | 11822133001 | 1 BOTTLE in 1 CARTON (11822-1330-1) > 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2019-06-06 | 0000-00-00 | No | No | Current |
| 11822-1330-2 | 11822133002 | 1 BOTTLE in 1 CARTON (11822-1330-2) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2019-06-06 | 0000-00-00 | No | No | Current |
| 11822-1330-3 | 11822133003 | 1 BOTTLE in 1 CARTON (11822-1330-3) > 90 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2022-01-17 | 0000-00-00 | No | No | Current |