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Citalopram HydrobromideDrug - Citalopram Hydrobromide The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Citalopram Hydrobromide
Strength -
EQ 20MG BASE
Applicant -
PUREPAC PHARM
New Drug Application (NDA) Number -
077033
Product Number -
002
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Oct 28, 2004
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Purepac Pharmaceutical Co
Citalopram Hydrobromide
Citalopram Hydrobromide Eq 20mg Base Tablet; Oral
Citalopram Hydrobromide Eq 40mg Base Tablet; Oral Citalopram Hydrobromide Eq 10mg Base Tablet; Oral Citalopram Hydrobromide Eq 20mg Base Tablet; Oral Citalopram Hydrobromide Eq 40mg Base Tablet; Oral Citalopram Hydrobromide Eq 10mg Base Tablet; Oral Citalopram Hydrobromide Eq 20mg Base Tablet; Oral Citalopram Hydrobromide Eq 20mg Base Tablet; Oral Citalopram Hydrobromide Eq 40mg Base Tablet; Oral Citalopram Hydrobromide Eq 10mg Base Tablet; Oral NewDrugInformation |