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ZoloftDrug - Zoloft The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Sertraline Hydrochloride
Strength -
EQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
Applicant -
PFIZER
New Drug Application (NDA) Number -
019839
Product Number -
004
Therapeutic Equivalence (TE) Code -
Approval Date -
Dec 30, 1991
Reference Listed Drug (RLD) -
No
Type -
DISCN
Applicant Full Name -
Pfizer Pharmaceuticals Inc
Zoloft
Zoloft Eq 20mg Base/ml Concentrate; Oral
Zoloft Eq 100mg Base Tablet; Oral Zoloft Eq 150mg Base **federal Register Determination That Product Was Not Discontinued Or Withdrawn For Safety Or Efficacy Reasons** Tablet; Oral Zoloft Eq 200mg Base **federal Register Determination That Product Was Not Discontinued Or Withdrawn For Safety Or Efficacy Reasons** Tablet; Oral Acthar Gel-synthetic 40 Units/ml Injectable; Injection Acthar Gel-synthetic 80 Units/ml Injectable; Injection Geref Eq 0.05mg Base/amp Injectable; Injection Geref Eq 0.5mg Base/vial Injectable; Injection Geref Eq 1mg Base/vial Injectable; Injection Ertaczo 2% Cream; Topical NewDrugInformation |