NDC 0832-0111 – Amantadine Hydrochloride

Amantadine Hydrochloride 100 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC0832-0111

Product details

Brand name
Amantadine Hydrochloride
Generic name
Amantadine hydrochloride
Labeler
Upsher-Smith Laboratories, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076186
Marketed since
December 15, 2011
Marketing end
February 29, 2028
Pharmacologic class
Influenza A M2 Protein Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Amantadine Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
0832-0111-00100 TABLET in 1 BOTTLE (0832-0111-00)Dec 15, 2011
0832-0111-50500 TABLET in 1 BOTTLE (0832-0111-50)Dec 15, 2011

Recalls mentioning this NDC

Other Amantadine Hydrochloride products