Amantadine Hydrochloride
- Product NDC
- 68788-7088
- 11-digit product format
- 687887088
- Labeler code
- 68788
- Product ID
- 68788-7088_1fce862d-3753-4a33-b78c-80b8d21f1f64
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amantadine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA074170
- Marketing category
- ANDA
- Marketing start
- 2018-01-26
- Marketing end
- 0000-00-00
- Substance
- AMANTADINE HYDROCHLORIDE
- Active strength
- 50 mg/5mL
- Pharmacologic classes
- Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record