NDC 71335-2664 – Amantadine Hydrochloride

Amantadine Hydrochloride 100 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2664

Product details

Brand name
Amantadine Hydrochloride
Generic name
Amantadine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA209171
Marketed since
June 12, 2017
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 (6)

Package NDCDescriptionSince
71335-2664-120 CAPSULE in 1 BOTTLE (71335-2664-1)Jun 26, 2025
71335-2664-230 CAPSULE in 1 BOTTLE (71335-2664-2)Jun 26, 2025
71335-2664-310 CAPSULE in 1 BOTTLE (71335-2664-3)Jun 26, 2025
71335-2664-414 CAPSULE in 1 BOTTLE (71335-2664-4)Jun 26, 2025
71335-2664-560 CAPSULE in 1 BOTTLE (71335-2664-5)Jun 26, 2025
71335-2664-6100 CAPSULE in 1 BOTTLE (71335-2664-6)Jun 26, 2025

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