NDC 10135-692 – Amantadine Hydrochloride

Amantadine Hydrochloride 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC10135-692

Product details

Brand name
Amantadine Hydrochloride
Generic name
Amantadine Hydrochloride
Labeler
Marlex Pharmaceuticals Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210215
Marketed since
March 1, 2020
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
10135-692-01100 TABLET in 1 BOTTLE (10135-692-01)Mar 1, 2020
10135-692-05500 TABLET in 1 BOTTLE (10135-692-05)Mar 1, 2020

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