NDC 17856-0646 – Amantadine Hydrochloride

Amantadine Hydrochloride 50 mg/5mL · Solution · Oral

Human Prescription Drug

Product NDC17856-0646

Product details

Brand name
Amantadine Hydrochloride
Generic name
Amantadine Hydrochloride
Labeler
ATLANTIC BIOLOGICALS CORP.
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
17856-0646-172 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0646-1) / 10 mL in 1 CUP, UNIT-DOSE (17856-0646-3)Apr 8, 2024
17856-0646-272 CUP, UNIT-DOSE in 1 PACKAGE (17856-0646-2) / 5 mL in 1 CUP, UNIT-DOSE (17856-0646-4)Apr 8, 2024

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