Basic Care Naproxen Sodium
- Product NDC
- 0113-7368
- 11-digit product format
- 001137368
- Labeler code
- 0113
- Product ID
- 0113-7368_4e098ef6-e0aa-4732-bec5-e87ed56a67a1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- L. Perrigo Company
- Application
- ANDA074661
- Marketing category
- ANDA
- Marketing start
- 2017-09-13
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 0113-7368-82 | 00113736882 | 1 BOTTLE in 1 CARTON (0113-7368-82) > 200 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2017-09-13 | 0000-00-00 | No | No | Current |
| 0113-7368-87 | 00113736887 | 300 TABLET, FILM COATED in 1 BOTTLE (0113-7368-87) | | 2017-09-13 | 0000-00-00 | No | No | Current |