basic care naproxen sodium
- Product NDC
- 0113-7033
- 11-digit product format
- 001137033
- Labeler code
- 0113
- Product ID
- 0113-7033_b12355d8-c36f-4af9-b981-e382cf0cff49
- 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
- 2019-01-23
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0113-7033-62 | 00113703362 | 1 BOTTLE in 1 CARTON (0113-7033-62) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2019-01-23 | 0000-00-00 | No | No | Current |
| 0113-7033-78 | 00113703378 | 1 BOTTLE in 1 CARTON (0113-7033-78) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2019-01-23 | 0000-00-00 | No | No | Current |