Diltiazem hydrochlorideextended-release capsule, coated, extended release

Ingredients and appearance - Product information

Diltiazem hydrochlorideextended-release capsule, coated, extended release- Diltiazem hydrochloride

Product information

Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC: 68788-7237
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Diltiazem hydrochloride ( UNII: OLH94387TE)( Diltiazem - UNII: EE92BBP03H ) 120 mgin 1

Inactive Ingredients

Ingredient Name Code
Ammonio methacrylate copolymer type a ( UNII: 8GQS4E66YY)
Ammonio methacrylate copolymer type b ( UNII: 161H3B14U2)
Ammonia ( UNII: 5138Q19F1X)
Gelatin, unspecified ( UNII: 2G86QN327L)
Hydroxypropyl cellulose (90000 wamw) ( UNII: UKE75GEA7F)
Propylene glycol ( UNII: 6DC9Q167V3)
Shellac ( UNII: 46N107B71O)
Sodium lauryl sulfate ( UNII: 368GB5141J)
Sucrose ( UNII: C151H8M554)
Talc ( UNII: 7SEV7J4R1U)
Titanium dioxide ( UNII: 15FIX9V2JP)
Triethyl citrate ( UNII: 8Z96QXD6UM)
Ferrosoferric oxide ( UNII: XM0M87F357)
Starch, corn ( UNII: O8232NY3SJ)

Product Characteristics

Color GRAY (light opaque body) Size 18 mm
Shape CAPSULE Score 1
Imprint Code par;C829

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
ANDA ANDA074984 USA

Labeler - Preferred Pharmaceutials Inc.( 791119022)

Establishment

Name ID/FEI Business Operations
Preferred Pharmaceutials Inc. 791119022 REPACK( 68788-7237)