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
71205-086_a2baa928-f954-40a1-a0e7-f7e373f5d3eb
Product NDC
71205-086
Form
CAPSULE
Composition / generic term
Minocycline Hydrochloride
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
19920201
Source listing expiry
20261231

Source-listed ingredients

  • MINOCYCLINE HYDROCHLORIDE — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 20 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-20) · 71205-086-20
  • 21 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-21) · 71205-086-21
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-30) · 71205-086-30
  • 60 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-60) · 71205-086-60
  • 90 CAPSULE in 1 BOTTLE, PLASTIC (71205-086-90) · 71205-086-90

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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