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#