Citalopram tablet, film coated

Ingredients and appearance - Product information

Citalopram tablet, film coated- Citalopram

Product information

Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC: 61919-288
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Citalopram hydrobromide ( UNII: I1E9D14F36)( Citalopram - UNII: 0DHU5B8D6V ) 10 mgin 1

Inactive Ingredients

Ingredient Name Code
Glycerin ( UNII: PDC6A3C0OX)
Lactose monohydrate ( UNII: EWQ57Q8I5X)
Polyvinyl alcohol ( UNII: 532B59J990)
Titanium dioxide ( UNII: 15FIX9V2JP)
Ferric oxide yellow ( UNII: EX438O2MRT)
Ferric oxide red ( UNII: 1K09F3G675)
Cellulose, microcrystalline ( UNII: OP1R32D61U)
Starch, corn ( UNII: O8232NY3SJ)
Magnesium stearate ( UNII: 70097M6I30)
Polyethylene glycols ( UNII: 3WJQ0SDW1A)
Sodium starch glycolate type a potato ( UNII: 5856J3G2A2)
Talc ( UNII: 7SEV7J4R1U)
Povidone k12 ( UNII: 333AG72FWJ)

Product Characteristics

Score 1 Imprint Code IP;52
Color orange Size 12 mm
Shape OVAL

Packaging

# Item Code Package Description Marketing Start Date
1 NDC: 61919-288-30 30 in 1 BOTTLE 2016/03/22

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
ANDA ANDA077289 USA 2016/03/22

Labeler - DIRECT RX( 079254320)

Establishment

Name ID/FEI Business Operations
DIRECT RX 079254320 repack( 61919-288)