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NilandronDrug - Nilandron The trade name of the product as shown on the labeling.
Dosage -
TABLET; ORAL
Active Ingredient(s) -
Nilutamide
Strength -
50MG
Applicant -
AVENTIS PHARMS
New Drug Application (NDA) Number -
020169
Product Number -
001
Therapeutic Equivalence (TE) Code -
Approval Date -
Sep 19, 1996
Reference Listed Drug (RLD) -
No
Type -
DISCN
Applicant Full Name -
Aventis Pharmaceuticals Inc
Nilandron
Procardia Xl 60mg Tablet, Extended Release; Oral
Procardia Xl 90mg Tablet, Extended Release; Oral Nilandron 150mg Tablet; Oral Nilandron 50mg Tablet; Oral Nifedipine 90mg Tablet, Extended Release; Oral Nifedipine 30mg Tablet, Extended Release; Oral Nifedipine 60mg Tablet, Extended Release; Oral Nifedipine 90mg Tablet, Extended Release; Oral Nifedipine 30mg Tablet, Extended Release; Oral Procardia Xl 30mg Tablet, Extended Release; Oral NewDrugInformation |