NDC 16571-834 – Amantadine Hydrochloride

Amantadine Hydrochloride 100 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC16571-834

Product details

Brand name
Amantadine Hydrochloride
Generic name
Amantadine Hydrochloride
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA210129
Marketed since
September 5, 2022
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
16571-834-01100 CAPSULE in 1 BOTTLE (16571-834-01)Sep 5, 2022
16571-834-50500 CAPSULE in 1 BOTTLE (16571-834-50)Sep 5, 2022

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