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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0440-7805
Application NumberANDA065062
Product Classification
M
Marketing Category
C73584
G
Generic Name
Minocycline hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateSeptember 25, 2013
FDA Product Classification
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