Memantine Hydrochloride
- Product NDC
- 47335-322
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Memantine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- ANDA090058
- Marketing category
- ANDA
- Substance
- MEMANTINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 47335-322-08 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-322-08) | 2015-07-11 | | No | Historical |
| 47335-322-13 | 500 TABLET, FILM COATED in 1 BOTTLE (47335-322-13) | 2015-07-11 | | No | Historical |
| 47335-322-18 | 1000 TABLET, FILM COATED in 1 BOTTLE (47335-322-18) | 2015-07-11 | | No | Historical |
| 47335-322-83 | 30 TABLET, FILM COATED in 1 BOTTLE (47335-322-83) | 2015-07-11 | | No | Historical |
| 47335-322-86 | 60 TABLET, FILM COATED in 1 BOTTLE (47335-322-86) | 2015-07-11 | | No | Historical |
| 47335-322-88 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-322-88) | 2015-07-11 | | No | Historical |