United States · FDA National Drug Code directory
Minocin
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 70842-160_07795bdf-7c92-445b-8b8b-d22c5c3eae7a
- Product NDC
- 70842-160
- Form
- INJECTION
- Composition / generic term
- minocycline hydrochloride
- Labeler
- Melinta Therapeutics, LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20130419
- Source listing expiry
- 20261231
Source-listed ingredients
- MINOCYCLINE HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 CARTON (70842-160-10) / 1 INJECTION in 1 VIAL (70842-160-01) · 70842-160-10
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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