Naproxen Sodium
- Product NDC
- 11822-0140
- 11-digit product format
- 118220140
- Labeler code
- 11822
- Product ID
- 11822-0140_d747b505-3939-4154-851e-cbd1b45a5c02
- 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
- 2016-07-01
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-0140-1 | 11822014001 | 270 TABLET, FILM COATED in 1 BOTTLE (11822-0140-1) | 2016-07-01 | 0000-00-00 | No | No | Current |