NDC 70710-1221 – Carbidopa

Carbidopa 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70710-1221

Product details

Brand name
Carbidopa
Generic name
Carbidopa
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209910
Marketed since
September 6, 2018
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Carbidopa →

Package NDC codes (1)

Package NDCDescriptionSince
70710-1221-1100 TABLET in 1 BOTTLE (70710-1221-1)Sep 6, 2018

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