NDC 68682-200 – Carbidopa

Carbidopa 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68682-200

Product details

Brand name
Carbidopa
Generic name
Carbidopa Tablets
Labeler
Oceanside Pharmaceuticals
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA017830
Marketed since
April 4, 2014
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Carbidopa →

Package NDC codes (1)

Package NDCDescriptionSince
68682-200-25100 TABLET in 1 BOTTLE (68682-200-25)Apr 4, 2014

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