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LeritineDrug - Leritine The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Anileridine Hydrochloride
Strength -
EQ 25MG BASE
Applicant -
MERCK
New Drug Application (NDA) Number -
010585
Product Number -
002
Therapeutic Equivalence (TE) Code -
Approval Date -
Approved Prior to Jan 1, 1982
Reference Listed Drug (RLD) -
No
Type -
DISCN
Applicant Full Name -
Merck And Co Inc
Leritine
Anagrelide Hcl Eq 1mg Base Capsule; Oral
Anagrelide Hcl Eq 0.5mg Base Capsule; Oral Anagrelide Hcl Eq 1mg Base Capsule; Oral Anagrelide Hcl Eq 0.5mg Base Capsule; Oral Anagrelide Hcl Eq 1mg Base Capsule; Oral Arimidex 1mg Tablet; Oral Leritine Eq 25mg Base Tablet; Oral Anagrelide Hcl Eq 0.5mg Base Capsule; Oral Anagrelide Hcl Eq 1mg Base Capsule; Oral Anagrelide Hcl Eq 0.5mg Base Capsule; Oral NewDrugInformation |