55154-8176 : Ondansetron Hydrochloride 4 mg Oral Tablet, Film Coated


NDC: 55154-8176
Labeler: Cardinal Health
Product Type: Human Prescription Drug
Drug Name:  Ondansetron Hydrochloride
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA078539
Rev. Date: 


Appearance:


Markings: F;91
Shapes:  Oval
Colors:  White
Size (mm): 6
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

F 91: (55154-8176) Ondansetron Hydrochloride 4 mg Oral Tablet, Film Coated by Cardinal Health
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

  • 55154-8176-0: 10 BLISTER PACK IN 1 BAG (55154‑8176‑0) > 1 TABLET, FILM COATED IN 1 BLISTER PACK

Active Ingredients:

  • Ondansetron Hydrochloride

Dosage Strength:

  • 4 mg

Inactive Ingredients:

  • Anhydrous Lactose
  • Microcrystalline Cellulose
  • Starch, Corn
  • Magnesium Stearate
  • Triacetin
  • Titanium Dioxide
  • Hypromellose 2910 (6 Mpa.s) /

Pharmaceutical Classes:

  • Serotonin 3 Receptor Antagonists [MoA]
  • Serotonin-3 Receptor Antagonist [EPC]

Related Products:

Based on records with the same trade name.
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  • 0409-4755 Ondansetron Hydrochloride 2 mg/ml Intramuscular; Intravenous Injection, Solution by Hospira, Inc.
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  • 0527-1726 Ondansetron Hydrochloride 2 mg/ml Intramuscular; Intravenous Injection by Lannett Company, Inc.
  • 0615-8185 Ondansetron Hydrochloride 4 mg Oral Tablet, Film Coated by Ncs Healthcare of Ky, Inc Dba Vangard Labs
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