ZOFRAN is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Novartis Pharmaceuticals Corporation. The primary component is Ondansetron Hydrochloride.
Product ID | 0078-0676_1ae5aba7-0e8c-40d6-9537-ceb096c07cda |
NDC | 0078-0676 |
Product Type | Human Prescription Drug |
Proprietary Name | ZOFRAN |
Generic Name | Ondansetron Hydrochloride |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2017-12-12 |
Marketing Category | NDA / NDA |
Application Number | NDA020103 |
Labeler Name | Novartis Pharmaceuticals Corporation |
Substance Name | ONDANSETRON HYDROCHLORIDE |
Active Ingredient Strength | 8 mg/1 |
Pharm Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2017-12-12 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA020103 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2017-12-12 |
Ingredient | Strength |
---|---|
ONDANSETRON HYDROCHLORIDE | 8 mg/1 |
SPL SET ID: | 555f81bc-4ce0-4f77-b394-b974838c4440 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
0078-0675 | ZOFRAN | ondansetron hydrochloride |
0078-0676 | ZOFRAN | ondansetron hydrochloride |
0078-0679 | ZOFRAN | ondansetron hydrochloride |
0078-0680 | ZOFRAN | ondansetron hydrochloride |
0173-0447 | ZOFRAN | ondansetron hydrochloride |
0173-0489 | ZOFRAN | ondansetron hydrochloride |
80425-0113 | Zofran | Zofran |
80425-0075 | Zofran | Zofran |
80425-0072 | Zofran | Zofran |
80425-0073 | Zofran | Zofran |
0143-2422 | Ondansetron | Ondansetron hydrochloride |
0143-2423 | Ondansetron | Ondansetron hydrochloride |
0179-0099 | ondansetron | ondansetron hydrochloride |
0179-0100 | ondansetron | ondansetron hydrochloride |
16714-671 | Ondansetron | Ondansetron Hydrochloride |
17856-0555 | Ondansetron | Ondansetron Hydrochloride |
0054-0064 | Ondansetron Hydrochloride | Ondansetron Hydrochloride |
0179-0247 | Ondansetron Hydrochloride | Ondansetron Hydrochloride |
0179-0248 | Ondansetron Hydrochloride | Ondansetron Hydrochloride |
0527-1726 | Ondansetron Hydrochloride | Ondansetron Hydrochloride |
0615-8185 | ondansetron hydrochloride | ondansetron hydrochloride |
0904-6551 | ondansetron hydrochloride | ondansetron hydrochloride |
0904-6552 | ondansetron hydrochloride | ondansetron hydrochloride |
10544-575 | Ondansetron Hydrochloride | Ondansetron Hydrochloride |
21695-834 | ONDANSETRON HYDROCHLORIDE | ONDANSETRON HYDROCHLORIDE |
21695-835 | ONDANSETRON HYDROCHLORIDE | ONDANSETRON HYDROCHLORIDE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ZOFRAN 73670524 1592702 Live/Registered |
GLAXO GROUP LIMITED 1987-07-06 |