CARBIDOPA AND LEVODOPA (68001-172)

Drug Facts

Product Profile

Brand Name CARBIDOPA AND LEVODOPA

Generic Name Carbidopa and Levodopa

Labeler BluePoint Laboratories

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

CARBIDOPA 50 mg/1, LEVODOPA 200 mg/1

Identifiers & Regulatory

Product NDC 68001-172

Product ID 68001-172_304c30d1-a315-0451-e063-6294a90abb9f

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA202323

Marketing Start 2014-01-22

Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68001172

Hyphenated Format 68001-172

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name CARBIDOPA AND LEVODOPA (source: ndc)

Generic Name Carbidopa and Levodopa (source: ndc)

Application Number ANDA202323 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

50 mg/1
200 mg/1

source: ndc

Packaging

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-172-00)

source: ndc

Packages (1)

68001-172-00 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-172-00)

Ingredients (2)

CARBIDOPA (50 mg/1) LEVODOPA (200 mg/1)

Linked Drug Pages (1)

CARBIDOPA AND LEVODOPA ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

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