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nifedipine

NDC 68682-109, nifedipine, tablet, film coated, extended release, from Oceanside Pharmaceuticals.

Product NDC
68682-109
Status
Listed
Labeler
Oceanside Pharmaceuticals
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075289
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68682-109 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NIFEDIPINE60 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68682-109-1068682010910100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-109-10)
68682-109-3068682010930300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-109-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c7874606-c71e-424c-b881-38697988e0d0

Use it

Look up 68682-109 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68682-109 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68682-109. 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.