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nifedipine

NDC 70807-503, nifedipine, tablet, film coated, extended release, from Elite Pharmaceutical Solution, Inc..

Product NDC
70807-503
Status
Listed
Labeler
Elite Pharmaceutical Solution, Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212016
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70807-503 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NIFEDIPINE90 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70807-503-1270807050312100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70807-503-12)
70807-503-1370807050313300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70807-503-13)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1df07edb-630d-4c70-a68c-bdbc607ce850

Use it

Look up 70807-503 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70807-503 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70807-503. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.