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Carbidopa and Levodopa

NDC 46708-332, Carbidopa and Levodopa, tablet, extended release, from Alembic Pharmaceuticals Limited.

Product NDC
46708-332
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210341
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-332 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CARBIDOPA25 mg/1
  • LEVODOPA100 mg/1

Pharmacologic classes

Amino Acids, Aromatic [CS]; Aromatic Amino Acid [EPC]

Package NDCNDC-11Package
46708-332-304670803323030 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-332-30)
46708-332-3146708033231100 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-332-31)
46708-332-91467080332911000 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-332-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a85a56c5-44dd-41d4-ac1c-bdc4758406a4

Use it

Look up 46708-332 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-332 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-332. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.