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Minocycline Hydrochloride

NDC 59651-339, Minocycline Hydrochloride, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
59651-339
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213662
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-339 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MINOCYCLINE HYDROCHLORIDE100 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
59651-339-505965103395050 TABLET, FILM COATED in 1 CONTAINER (59651-339-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/799a9871-3249-471e-b88d-5d8f7d4b96ad

  • NADAC price for package 59651033950

    GET /v1/drugs/nadac/59651033950

Use it

Look up 59651-339 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-339 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-339. 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.