Naproxen Sodium
- Product NDC
- 49035-903
- 11-digit product format
- 490350903
- Labeler code
- 49035
- Product ID
- 49035-903_f158f04a-13c6-41cb-b574-875f9b0fbcc1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Naproxen Sodium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Wal-Mart Stores Inc
- Application
- ANDA204872
- Marketing category
- ANDA
- Marketing start
- 2017-01-23
- Marketing end
- 2023-02-09
- Substance
- 2-NAPHTHALENEACETIC ACID, 6-METHOXY-.ALPHA.-METHYL-, SODIUM SALT, (S)-
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49035-903-10 | 49035090310 | 1 BOTTLE, PLASTIC in 1 CARTON (49035-903-10) > 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 2017-01-23 | 0000-00-00 | No | No | Current |
| 49035-903-12 | 49035090312 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49035-903-12) | 2017-01-23 | 0000-00-00 | No | No | Current |