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Nifedipine

NDC 46708-732, Nifedipine, tablet, extended release, from Alembic Pharmaceuticals Limited.

Product NDC
46708-732
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216896
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-732 \
  -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
46708-732-3146708073231100 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-732-31)
46708-732-6346708073263300 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-732-63)
46708-732-91467080732911000 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-732-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1486f187-0ec6-4c70-8991-02c1493912b4

Use it

Look up 46708-732 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-732 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-732. 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.