Lisinopril and hydrochlorothiazide tablet

Ingredients and appearance - Product information

Lisinopril and hydrochlorothiazide tablet- Lisinopril and hydrochlorothiazide

Product information

Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC: 42708-034
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Lisinopril ( UNII: E7199S1YWR)( Lisinopril anhydrous - UNII: 7Q3P4BS2FD ) 10 mgin 1
Hydrochlorothiazide ( UNII: 0J48LPH2TH)( Hydrochlorothiazide - UNII: 0J48LPH2TH ) 12.5 mgin 1

Inactive Ingredients

Ingredient Name Code
Silicon dioxide ( UNII: ETJ7Z6XBU4)
Dibasic calcium phosphate dihydrate ( UNII: O7TSZ97GEP)
Fd&c red no. 40 ( UNII: WZB9127XOA)
Magnesium stearate ( UNII: 70097M6I30)
Mannitol ( UNII: 3OWL53L36A)
Starch, corn ( UNII: O8232NY3SJ)

Product Characteristics

Color PINK Size 8 mm
Shape ROUND Score 1
Imprint Code WATSON;860

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
ANDA ANDA076194 USA

Labeler - QPharma Inc( 030620888)

Establishment

Name ID/FEI Business Operations
QPharma Inc 030620888 REPACK( 42708-034)