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AmoxapineDrug - Amoxapine The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Amoxapine
Strength -
100MG
Applicant -
WATSON LABS
New Drug Application (NDA) Number -
072420
Product Number -
001
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
May 11, 1989
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Watson Laboratories Inc
Amoxapine
Ammonium Lactate Eq 12% Base Lotion; Topical
Ammonium Lactate Eq 12% Base Lotion; Topical Ammonium Lactate Eq 12% Base Lotion; Topical Lac-hydrin Eq 12% Base Lotion; Topical Camoquin Hcl Eq 200mg Base Tablet; Oral Amoxapine 100mg Tablet; Oral Amoxapine 150mg Tablet; Oral Amoxapine 25mg Tablet; Oral Amoxapine 50mg Tablet; Oral Amoxapine 100mg Tablet; Oral NewDrugInformation |