basic care naproxen sodium pm
- Product NDC
- 0113-7264
- 11-digit product format
- 001137264
- Labeler code
- 0113
- Product ID
- 0113-7264_6431fba1-429b-43ab-9ac1-3e8d1669bffd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- diphenhydramine hydrochloride, naproxen sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- L. Perrigo Company
- Application
- ANDA208499
- Marketing category
- ANDA
- Marketing start
- 2020-01-09
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM
- Active strength
- 25 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 0113-7264-06 | 00113726406 | 1 BOTTLE in 1 CARTON (0113-7264-06) > 160 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2020-01-09 | 0000-00-00 | No | No | Current |