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Nifedipine

NDC 70771-1190, Nifedipine, tablet, extended release, from Zydus Lifesciences Limited.

Product NDC
70771-1190
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210012
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1190 \
  -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
70771-1190-0707711190001000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1190-0)
70771-1190-170771119001100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1190-1)
70771-1190-370771119003300 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1190-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ac3f68b2-29b5-45c1-b6a2-54704dc3143e

Use it

Look up 70771-1190 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1190 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1190. 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.