Amantadine Hydrochloride
- Product NDC
- 0527-1868
- 11-digit product format
- 005271868
- Labeler code
- 0527
- Product ID
- 0527-1868_aac34664-21c1-4d1f-81ba-3f3309efbe2f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amantadine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA209221
- Marketing category
- ANDA
- Marketing start
- 2017-06-15
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#