Desipramine Hydrochloride
Desipramine Hydrochloride Tablets, USP
Approved
Approval ID
f3127fff-2943-424d-8b8b-80aa320a2d07
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 17, 2011
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.
Desipramine Hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code21695-428
Application NumberANDA072100
Product Classification
M
Marketing Category
C73584
G
Generic Name
Desipramine Hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateJune 20, 2007
FDA Product Classification
INGREDIENTS (9)
DESIPRAMINE HYDROCHLORIDEActive
Quantity: 25 mg in 1 1
Code: 1Y58DO4MY1
Classification: ACTIB
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
HYPROMELLOSE 2910 (3 MPA.S)Inactive
Code: 0VUT3PMY82
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
HYDROXYPROPYL CELLULOSEInactive
Code: RFW2ET671P
Classification: IACT
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
POLYETHYLENE GLYCOLInactive
Code: 3WJQ0SDW1A
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT