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Nifedipine

NDC 68682-105, Nifedipine, tablet, extended release, from Oceanside Pharmaceuticals.

Product NDC
68682-105
Status
Listed
Labeler
Oceanside Pharmaceuticals
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075269
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68682-105 \
  -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
68682-105-1068682010510100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-105-10)
68682-105-3068682010530300 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-105-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cb051508-60f3-4b89-9da0-5261024bd7f4

Use it

Look up 68682-105 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68682-105 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68682-105. 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.