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Nifedipine

NDC 50742-620, nifedipine, tablet, extended release, from Ingenus Pharmaceuticals, LLC.

Product NDC
50742-620
Status
Listed
Labeler
Ingenus Pharmaceuticals, LLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202987
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50742-620 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NIFEDIPINE30 mg/1

Pharmacologic classes

Calcium Channel Antagonists [MoA]; Dihydropyridine Calcium Channel Blocker [EPC]; Dihydropyridines [CS]

Package NDCNDC-11Package
50742-620-0150742062001100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-620-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4d02eba2-e964-4fa7-aaae-25949b5f0316

  • NADAC price for package 50742062001

    GET /v1/drugs/nadac/50742062001

Use it

Look up 50742-620 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50742-620 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50742-620. 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.