45963-479 : Alosetron Hydrochloride .5 mg Oral Tablet


NDC: 45963-479
Labeler: Actavis Pharma, Inc.
Product Type: Human Prescription Drug
Drug Name:  Alosetron Hydrochloride
Dosage Form: Oral Tablet
Application #: NDA021107
Rev. Date: 


Appearance:


Markings: GX;EX1
Shapes:  Oval
Colors:  White
Size (mm): 11
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.

NDC Package Codes:

  • 45963-479-03: 1 BOTTLE IN 1 CARTON (45963‑479‑03) > 30 TABLET IN 1 BOTTLE

Active Ingredients:

  • Alosetron Hydrochloride

Dosage Strength:

  • .5 mg

Inactive Ingredients:

  • Lactose
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Starch, Corn
  • Hypromelloses
  • Titanium Dioxide
  • Triacetin

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 45963-480 Alosetron Hydrochloride 1 mg Oral Tablet by Actavis Pharma, Inc.
  • 0054-0295 Alosetron Hydrochloride .5 mg Oral Tablet by Roxane Laboratories, Inc.
  • 0054-0296 Alosetron Hydrochloride 1 mg Oral Tablet by Roxane Laboratories, Inc.
  • 42291-123 Alosetron Hydrochloride .5 mg Oral Tablet, Film Coated by Avkare, Inc.
  • 42291-124 Alosetron Hydrochloride 1 mg Oral Tablet, Film Coated by Avkare, Inc.
  • 49884-819 Alosetron Hydrochloride .5 mg Oral Tablet by Par Pharmaceutical, Inc.
  • 49884-820 Alosetron Hydrochloride 1 mg Oral Tablet by Par Pharmaceutical, Inc.
  • 53746-248 Alosetron Hydrochloride .5 mg Oral Tablet, Film Coated by Amneal Pharmaceuticals of New York LLC
  • 53746-249 Alosetron Hydrochloride 1 mg Oral Tablet, Film Coated by Amneal Pharmaceuticals of New York LLC
  • 65162-248 Alosetron Hydrochloride .5 mg Oral Tablet, Film Coated by Amneal Pharmaceuticals LLC
  • 65162-249 Alosetron Hydrochloride 1 mg Oral Tablet, Film Coated by Amneal Pharmaceuticals LLC

NDC QR Code

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NDC 45963-479 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.