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NimotopDrug - Nimotop The trade name of the product as shown on the labeling.
Dosage -
CAPSULE; ORAL
Active Ingredient(s) -
Nimodipine
Strength -
30MG
Applicant -
BAYER PHARMS
New Drug Application (NDA) Number -
018869
Product Number -
001
Therapeutic Equivalence (TE) Code -
Approval Date -
Dec 28, 1988
Reference Listed Drug (RLD) -
Yes
Type -
RX
Applicant Full Name -
Bayer Pharmaceuticals Corp
Nimotop
Procardia Xl 60mg Tablet, Extended Release; Oral
Procardia Xl 90mg Tablet, Extended Release; Oral Nilandron 150mg Tablet; Oral Nilandron 50mg Tablet; Oral Nimotop 30mg Capsule; 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 |