Verapamil hydrochloride capsule, delayed release pellets

Ingredients and appearance - Product information

Verapamil hydrochloride capsule, delayed release pellets- Verapamil hydrochloride

Product information

Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC: 68788-6757
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Verapamil hydrochloride ( UNII: V3888OEY5R)( Verapamil - UNII: CJ0O37KU29 ) 120 mgin 1

Inactive Ingredients

Ingredient Name Code
Fumaric acid ( UNII: 88XHZ13131)
Talc ( UNII: 7SEV7J4R1U)
Sucrose ( UNII: C151H8M554)
Starch, corn ( UNII: O8232NY3SJ)
Povidones ( UNII: FZ989GH94E)
Shellac ( UNII: 46N107B71O)
Gelatin ( UNII: 2G86QN327L)
Fd&c red no. 40 ( UNII: WZB9127XOA)
Ferric oxide yellow ( UNII: EX438O2MRT)
Titanium dioxide ( UNII: 15FIX9V2JP)
Methylparaben ( UNII: A2I8C7HI9T)
Propylparaben ( UNII: Z8IX2SC1OH)
Silicon dioxide ( UNII: ETJ7Z6XBU4)
Sodium lauryl sulfate ( UNII: 368GB5141J)

Product Characteristics

Color YELLOW Size 18 mm
Shape CAPSULE Score 1
Imprint Code 60274;120;mg

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
NDA NDA019614 USA

Labeler - Preferred Pharmaceuticals, Inc.( 791119022)

Establishment

Name ID/FEI Business Operations
Preferred Pharmaceuticals, Inc. 791119022 RELABEL( 68788-6757)