NDC 0121-0646 – Amantadine Hydrochloride

Amantadine Hydrochloride 50 mg/5mL · Solution · Oral

Human Prescription Drug

Product NDC0121-0646

Product details

Brand name
Amantadine Hydrochloride
Generic name
Amantadine Hydrochloride
Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA074509
Marketed since
July 17, 1995
Listing expires
December 31, 2026
Pharmacologic class
Influenza A M2 Protein Inhibitor

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
0121-0646-1010 TRAY in 1 CASE (0121-0646-10) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSEJul 17, 1995
0121-0646-16473 mL in 1 BOTTLE (0121-0646-16)Jul 17, 1995

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