ANZEMET is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Validus Pharmaceuticals Llc. The primary component is Dolasetron Mesylate.
Product ID | 30698-121_fc7a7002-d1d6-40f2-9a44-44ce51686152 |
NDC | 30698-121 |
Product Type | Human Prescription Drug |
Proprietary Name | ANZEMET |
Generic Name | Dolasetron Mesylate |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 1997-09-11 |
Marketing Category | NDA / NDA |
Application Number | NDA020623 |
Labeler Name | Validus Pharmaceuticals LLC |
Substance Name | DOLASETRON MESYLATE |
Active Ingredient Strength | 100 mg/1 |
Pharm Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 1997-09-11 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA020623 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1997-09-11 |
Ingredient | Strength |
---|---|
DOLASETRON MESYLATE | 100 mg/1 |
SPL SET ID: | 201b0eb8-4a1e-4e22-ab4b-addb642710d6 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
30698-120 | ANZEMET | dolasetron mesylate |
30698-121 | ANZEMET | dolasetron mesylate |
30698-220 | ANZEMET | dolasetron mesylate |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ANZEMET 74343289 1863035 Live/Registered |
U.S. PHARMACEUTICALS HOLDINGS II, LLC 1992-12-28 |