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Minocycline Hydrochloride

NDC 67877-436, Minocycline Hydrochloride, tablet, film coated, extended release, from Ascend Laboratories, LLC.

Product NDC
67877-436
Status
Listed
Labeler
Ascend Laboratories, LLC
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/67877-436 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MINOCYCLINE HYDROCHLORIDE55 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
67877-436-0167877043601100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-436-01)
67877-436-0567877043605500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-436-05)
67877-436-146787704361410 BLISTER PACK in 1 CARTON (67877-436-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
67877-436-306787704363030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-436-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a8f95207-b259-4f50-87f2-3652d9268890

Use it

Look up 67877-436 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67877-436 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67877-436. 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.