NDC 30698-220

ANZEMET

Dolasetron Mesylate

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: 30698-220_3b3a8574-591c-46b7-99cc-adca27a22c01
• NDC: 30698-220
• 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 /
• Application Number: NDA020623
• Labeler Name: Validus Pharmaceuticals LLC
• Substance Name: DOLASETRON MESYLATE
• Active Ingredient Strength: 50 mg/1
• Pharm Classes: Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 30698-220-10

10 TABLET, FILM COATED in 1 BOTTLE (30698-220-10)

• Marketing Start Date: 1997-09-11
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "ANZEMET" or generic name "Dolasetron Mesylate"

NDC	Brand Name	Generic Name
30698-120	ANZEMET	dolasetron mesylate
30698-121	ANZEMET	dolasetron mesylate
30698-220	ANZEMET	dolasetron mesylate