Menstridol
- Product NDC
- 0280-0270
- 11-digit product format
- 002800270
- Labeler code
- 0280
- Product ID
- 0280-0270_d46a195c-cf36-4a1d-e053-2995a90ad54d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- NAPROXEN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bayer HealthCare LLC.
- Application
- NDA020204
- Marketing category
- NDA
- Marketing start
- 2014-07-01
- Marketing end
- 0000-00-00
- Substance
- NAPROXEN SODIUM
- Active strength
- 220 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 0280-0270-20 | 00280027020 | 4 BLISTER PACK in 1 CARTON (0280-0270-20) > 5 TABLET in 1 BLISTER PACK | 4 blister pack | 2014-07-01 | 0000-00-00 | No | No | Current |