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CARBIDOPA AND LEVODOPA

NDC 62756-985, CARBIDOPA AND LEVODOPA, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-985
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078536
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62756-985 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CARBIDOPA25 mg/1
  • LEVODOPA250 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
62756-985-0162756098501100 TABLET in 1 BOTTLE (62756-985-01)
62756-985-0262756098502500 TABLET in 1 BOTTLE (62756-985-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/829c35f9-ace0-11dd-8800-f3e252b43544

Use it

Look up 62756-985 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-985 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-985. 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.