NDC 62135-322 – Methyldopa

Methyldopa 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC62135-322

Product details

Brand name
Methyldopa
Generic name
Methyldopa
Labeler
Chartwell RX, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA018934
Marketed since
June 29, 1984
Listing expires
December 31, 2026
Pharmacologic class
Central alpha-2 Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Methyldopa →

Package NDC codes (2)

Package NDCDescriptionSince
62135-322-18180 TABLET, FILM COATED in 1 BOTTLE (62135-322-18)Nov 22, 2022
62135-322-9090 TABLET, FILM COATED in 1 BOTTLE (62135-322-90)Nov 22, 2022

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