NDC 46708-333 – Carbidopa and Levodopa

Carbidopa 50 mg/1; Levodopa 200 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC46708-333

Product details

Brand name
Carbidopa and Levodopa
Generic name
Carbidopa and Levodopa
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210341
Marketed since
June 6, 2019
Listing expires
December 31, 2026
Pharmacologic class
Aromatic Amino Acid

Active ingredients

Uses, dosage, side effects and warnings for Carbidopa and Levodopa →

Package NDC codes (3)

Package NDCDescriptionSince
46708-333-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-333-30)Jun 6, 2019
46708-333-31100 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-333-31)Jun 6, 2019
46708-333-911000 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-333-91)Jun 6, 2019

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