Minocycline Hydrochloride
MINOCYCLINE HYDROCHLORIDE CAPSULES, USPRx only
Approved
Approval ID
a74f9195-8a43-428f-9262-a41313165e0a
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 6, 2010
Manufacturers
FDA
Rebel Distributors Corp.
DUNS: 118802834
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 Code21695-693
Application NumberANDA065062
Product Classification
M
Marketing Category
C73584
G
Generic Name
Minocycline Hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateMay 1, 2007
FDA Product Classification
INGREDIENTS (6)
minocycline hydrochlorideActive
Quantity: 50 mg in 1 1
Code: 0020414E5U
Classification: ACTIB
FERROSOFERRIC OXIDEInactive
Code: XM0M87F357
Classification: IACT
magnesium stearateInactive
Code: 70097M6I30
Classification: IACT
gelatinInactive
Code: 2G86QN327L
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
titanium dioxideInactive
Code: 15FIX9V2JP
Classification: IACT