United States · FDA National Drug Code directory

Minocycline Hydrochloride

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: 68180-379_ad320f99-9382-4ef0-b6b6-86542020555a
Product NDC: 68180-379
Form: TABLET, EXTENDED RELEASE
Composition / generic term: Minocycline Hydrochloride
Labeler: Lupin Pharmaceuticals, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20120214
Source listing expiry: 20261231

Source-listed ingredients

MINOCYCLINE HYDROCHLORIDE — 45 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

Package details are not available in this snapshot.

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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