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NDC 68788-9368-02 Ondansetron Hydrochloride 4 mg/1 Details
Ondansetron Hydrochloride 4 mg/1
Ondansetron Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is ONDANSETRON HYDROCHLORIDE.
Product Information
NDC | 68788-9368 |
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Product ID | 68788-9368_d4ce06ae-a386-41a4-828c-72391dda6f7d |
Associated GPIs | 50250065050310 |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Ondansetron Hydrochloride |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Ondansetron Hydrochloride |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET, FILM COATED |
Route | ORAL |
Active Ingredient Strength | 4 |
Active Ingredient Units | mg/1 |
Substance Name | ONDANSETRON HYDROCHLORIDE |
Labeler Name | Preferred Pharmaceuticals, Inc. |
Pharmaceutical Class | Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA078539 |
Listing Certified Through | 2024-12-31 |
Package
NDC 68788-9368-02 (68788936802)
NDC Package Code | 68788-9368-2 |
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Billing NDC | 68788936802 |
Package | 12 TABLET, FILM COATED in 1 BOTTLE (68788-9368-2) |
Marketing Start Date | 2017-06-23 |
NDC Exclude Flag | N |
Pricing Information | N/A |