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Minocycline Hydrochloride

NDC 70518-1336, Minocycline Hydrochloride, capsule, from REMEDYREPACK INC..

Product NDC
70518-1336
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA065470
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1336 \
  -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
70518-1336-17051813360130 CAPSULE in 1 BLISTER PACK (70518-1336-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0becbde8-6ec5-4830-a0d9-cfdb7b15eb84

Use it

Look up 70518-1336 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1336 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-1336. 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.