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Nifedipine

NDC 68382-685, Nifedipine, tablet, extended release, from Zydus Pharmaceuticals (USA) Inc..

Product NDC
68382-685
Status
Listed
Labeler
Zydus Pharmaceuticals (USA) Inc.
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/68382-685 \
  -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
68382-685-0168382068501100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-685-01)
68382-685-10683820685101000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-685-10)
68382-685-9568382068595300 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-685-95)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/657221d5-9eb8-42f9-8cdc-39cefc386f51

Use it

Look up 68382-685 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-685 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-685. 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.