Naproxen Sodium
- Product NDC
- 30142-177
- 11-digit product format
- 301420177
- Labeler code
- 30142
- Product ID
- 30142-177_bdcd86be-0ae3-4bf6-ba20-4b5080197a8d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- ANDA074661
- Marketing category
- ANDA
- Marketing start
- 2005-02-08
- Marketing end
- 2023-04-30
- 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
- 0000-00-00
- 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 |
|---|
| 30142-177-82 | 30142017782 | 200 TABLET, FILM COATED in 1 BOTTLE (30142-177-82) | 2005-02-08 | 0000-00-00 | No | No | Current |