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Minocycline Hydrochloride

NDC 72789-525, Minocycline Hydrochloride, tablet, film coated, extended release, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-525
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204453
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72789-525 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MINOCYCLINE HYDROCHLORIDE90 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72789-525-307278905253030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-525-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3e74e8a3-2670-97f5-e063-6394a90a361e

Use it

Look up 72789-525 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-525 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-525. 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.