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CARBIDOPA AND LEVODOPA

NDC 62756-461, CARBIDOPA AND LEVODOPA, tablet, extended release, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-461
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077828
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62756-461 \
  -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
62756-461-0862756046108100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-461-08)
62756-461-18627560461181000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-461-18)
62756-461-836275604618330 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-461-83)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d2a64f14-f638-49d9-8a96-cb7ae46ac3ea

Use it

Look up 62756-461 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-461 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-461. 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.