amantadine hydrochloride
- Product NDC
- 59746-699
- 11-digit product format
- 597460699
- Labeler code
- 59746
- Product ID
- 59746-699_8743abcd-9667-46e1-b60c-997b6f4238f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amantadine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Jubilant Cadista Pharmaceuticals Inc.
- Application
- ANDA210403
- Marketing category
- ANDA
- Marketing start
- 2018-02-07
- Marketing end
- 0000-00-00
- Substance
- AMANTADINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 59746-699-01 | 59746069901 | 100 TABLET, FILM COATED in 1 BOTTLE (59746-699-01) | 2018-02-07 | 0000-00-00 | No | No | Current |
| 59746-699-05 | 59746069905 | 500 TABLET, FILM COATED in 1 BOTTLE (59746-699-05) | 2018-02-07 | 0000-00-00 | No | No | Current |
| 59746-699-30 | 59746069930 | 30 TABLET, FILM COATED in 1 BOTTLE (59746-699-30) | 2018-02-07 | 0000-00-00 | No | No | Current |