NDC 16714-067 – Carbidopa

Carbidopa 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC16714-067

Product details

Brand name
Carbidopa
Generic name
Carbidopa
Labeler
NorthStar Rx LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211055
Marketed since
October 21, 2019
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Carbidopa →

Package NDC codes (1)

Package NDCDescriptionSince
16714-067-01100 TABLET in 1 BOTTLE (16714-067-01)Oct 21, 2019

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