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Minocycline hydrochloride

MINOCYCLINE 100 MG 60 CAPS FOR OHM

Approved
Approval ID

0b0cce68-5643-4239-82c7-105f5077a0e0

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Sep 25, 2013

Manufacturers
FDA

Liberty Pharmaceuticals, Inc.

DUNS: 012568840

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Minocycline hydrochloride

PRODUCT DETAILS

NDC Product Code0440-7805
Application NumberANDA065062
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateSeptember 25, 2013
Generic NameMinocycline hydrochloride

INGREDIENTS (9)

MINOCYCLINE HYDROCHLORIDEActive
Quantity: 100 mg in 1 1
Code: 0020414E5U
Classification: ACTIM
GELATINInactive
Code: 2G86QN327L
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
POTASSIUM HYDROXIDEInactive
Code: WZH3C48M4T
Classification: IACT
PROPYLENE GLYCOLInactive
Code: 6DC9Q167V3
Classification: IACT
SHELLACInactive
Code: 46N107B71O
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
FERROSOFERRIC OXIDEInactive
Code: XM0M87F357
Classification: IACT

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Minocycline hydrochloride - FDA Drug Approval Details