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Minocycline Hydrochloride

NDC 68180-379, Minocycline Hydrochloride, tablet, extended release, from Lupin Pharmaceuticals, Inc..

Product NDC
68180-379
Status
Listed
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091424
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68180-379 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MINOCYCLINE HYDROCHLORIDE45 mg/1

Pharmacologic classes

Decreased Prothrombin Activity [PE]; Tetracycline-class Drug [EPC]; Tetracyclines [CS]

Package NDCNDC-11Package

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3b1e1cf1-ebd2-4aba-a219-9f9939fdb03b

Use it

Look up 68180-379 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68180-379 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68180-379. 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.