0093-0233 : Ondansetron 4 mg (Ondansetron Hydrochloride Dihydrate 5 mg) Oral Tablet


NDC: 0093-0233
Labeler: Teva Pharmaceuticals USA Inc
Product Type: Human Prescription Drug
Drug Name:  Ondansetron Hydrochloride
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA076252
Rev. Date: 


Appearance:


Markings: 93;233
Shapes:  Round
Colors:  White
Size (mm): 7
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.

93 233: (0093-0233) Ondansetron 4 mg (Ondansetron Hydrochloride Dihydrate 5 mg) Oral Tablet by Teva Pharmaceuticals USA Inc
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:

  • 0093-0233-56: 30 TABLET, FILM COATED IN 1 BOTTLE (0093‑0233‑56)

Active Ingredients:

  • Ondansetron Hydrochloride

Dosage Strength:

  • 4 mg

Inactive Ingredients:

  • Hypromellose 2910 (5 Mpa.s)
  • Lactose Monohydrate
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Starch, Corn
  • Polyethylene Glycol 6000
  • Polyethylene Glycol 400
  • Sodium Starch Glycolate Type a Potato
  • Titanium Dioxide

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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  • 0054-0064 Ondansetron Hydrochloride 4 mg/5ml Oral Solution by Roxane Laboratories, Inc
  • 0069-1340 Ondansetron Hydrochloride 2 mg/ml Intramuscular; Intravenous Injection, Solution by Pfizer Laboratories Div Pfizer Inc
  • 0179-0099 Ondansetron 4 mg (Ondansetron Hydrochloride Dihydrate 5 mg) Oral Tablet by Kaiser Foundation Hospitals
  • 0179-0100 Ondansetron 8 mg (As Ondansetron Hydrochloride Dihydrate 10 mg) Oral Tablet by Kaiser Foundation Hospitals
  • 0179-0247 Ondansetron Hydrochloride 4 mg Oral Tablet, Film Coated by Kaiser Foundation Hospitals
  • 0179-0248 Ondansetron Hydrochloride 8 mg Oral Tablet, Film Coated by Kaiser Foundation Hospitals
  • 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
  • 0781-1679 Ondansetron 4 mg (Ondansetron Hydrochloride Dihydrate 5 mg) Oral Tablet by Sandoz Inc
  • 0781-1681 Ondansetron 8 mg (As Ondansetron Hydrochloride Dihydrate 10 mg) Oral Tablet by Sandoz Inc
  • 0781-1879 Ondansetron 24 mg (Ondansetron Hydrochloride Dihydrate 30 mg) Oral Tablet by Sandoz Inc
  • 0904-6551 Ondansetron Hydrochloride 4 mg Oral Tablet, Film Coated by Major Pharmaceuticals
  • 0904-6552 Ondansetron Hydrochloride 8 mg Oral Tablet, Film Coated by Major Pharmaceuticals
  • 10544-575 Ondansetron Hydrochloride 8 mg Oral Tablet, Film Coated by Blenheim Pharmacal, Inc.
  • 21695-834 Ondansetron 4 mg (Ondansetron Hydrochloride Dihydrate 5 mg) Oral Tablet by Rebel Distributors Corp
  • 21695-835 Ondansetron 8 mg (As Ondansetron Hydrochloride Dihydrate 10 mg) Oral Tablet by Rebel Distributors Corp
  • 23155-168 Ondansetron Hydrochloride 2 mg/ml Intravenous Injection, Solution by Heritage Pharmaceuticals Inc.
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NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.