Naproxen sodium
- Product NDC
- 50090-4704
- 11-digit product format
- 500904704
- Labeler code
- 50090
- Product ID
- 50090-4704_cfd0d5d2-d722-41ad-84b9-9e22f43107d6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA207612
- Marketing category
- ANDA
- Marketing start
- 2019-12-11
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50090-4704-0 | 50090470400 | 30 TABLET in 1 BOTTLE (50090-4704-0) | 30 tablet | 2019-12-11 | 0000-00-00 | No | No | Current |