Naproxen Sodium
- Product NDC
- 69168-632
- 11-digit product format
- 691680632
- Labeler code
- 69168
- Product ID
- 69168-632_e7259700-488e-4132-b906-973a557f8c97
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium 220mg
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Allegiant Health
- Application
- ANDA090545
- Marketing category
- ANDA
- Marketing start
- 2014-12-23
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69168-632-84 | 69168063284 | 1 BOTTLE in 1 CARTON (69168-632-84) > 50 TABLET, COATED in 1 BOTTLE | 1 bottle | 2014-12-23 | 0000-00-00 | No | No | Current |