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minocycline hydrochloride

NDC 68382-531, minocycline hydrochloride, tablet, extended release, from Zydus Pharmaceuticals (USA) Inc..

Product NDC
68382-531
Status
Listed
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203553
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68382-531 \
  -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
68382-531-0168382053101100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-01)
68382-531-0568382053105500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-05)
68382-531-066838205310630 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-06)
68382-531-10683820531101000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-10)
68382-531-166838205311690 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-16)
68382-531-306838205313010 BLISTER PACK in 1 CARTON (68382-531-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/85f082a5-bba1-4441-ba28-4b8ec9a537f2

Use it

Look up 68382-531 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-531 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-531. 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.