68788-9892 : Ondansetron 8 mg (As Ondansetron Hydrochloride Dihydrate 10 mg) Oral Tablet


NDC: 68788-9892
Labeler: Preferred Pharmaceuticals, Inc
Product Type: Human Prescription Drug
Drug Name:  Ondansetron Hydrochloride
Dosage Form: Oral Tablet
Application #: ANDA077851
Rev. Date: 


Appearance:


Markings: 8;NO
Shapes:  Oval
Colors:  Yellow
Size (mm): 12
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.

8 NO: (63304-459) Ondansetron 8 mg (As Ondansetron Hydrochloride Dihydrate 10 mg) Oral Tablet by Preferred Pharmaceuticals, 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:

  • 68788-9892-1: 10 TABLET IN 1 BOTTLE (68788‑9892‑1)
  • 68788-9892-3: 30 TABLET IN 1 BOTTLE (68788‑9892‑3)

Active Ingredients:

  • Ondansetron Hydrochloride

Dosage Strength:

  • 8 mg

Inactive Ingredients:

  • Lactose Monohydrate
  • Cellulose, Microcrystalline
  • Croscarmellose Sodium
  • Starch, Corn
  • Magnesium Stearate
  • Hypromelloses
  • Triacetin
  • Ferric Oxide Yellow

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 68788-9893 Ondansetron 4 mg (Ondansetron Hydrochloride Dihydrate 5 mg) Oral Tablet by Preferred Pharmaceuticals, Inc
  • 68788-8418 Ondansetron Hydrochloride 4 mg Oral Tablet, Film Coated by Preferred Pharmaceuticals Inc.
  • 68788-8582 Ondansetron Hydrochloride 8 mg Oral Tablet, Film Coated by Preferred Pharmaceuticals Inc.
  • 68788-8651 Ondansetron Hydrochloride 4 mg Oral Tablet, Film Coated by Preferred Pharmaceuticals Inc.
  • 68788-9368 Ondansetron Hydrochloride 4 mg Oral Tablet, Film Coated by Preferred Pharmaceuticals, Inc.
  • 68788-9402 Ondansetron Hydrochloride 8 mg Oral Tablet, Film Coated by Preferred Pharmaceuticals, Inc.
  • 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
  • 0093-0233 Ondansetron 4 mg (Ondansetron Hydrochloride Dihydrate 5 mg) Oral Tablet by Teva Pharmaceuticals USA Inc
  • 0093-7236 Ondansetron 8 mg (As Ondansetron Hydrochloride Dihydrate 10 mg) Oral Tablet by Teva Pharmaceuticals USA 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.
  • 0409-4759 Ondansetron Hydrochloride 2 mg/ml Intramuscular; Intravenous Injection, Solution by Hospira, Inc.
  • 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
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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.