51672-4138 : Granisetron 1 mg (Granisetron Hydrochloride 1.12 mg) Oral Tablet


NDC51672-4138
Labeler: Taro Pharmaceuticals U.S.a., Inc.
Product Type: Human Prescription Drug
Drug Name:  Granisetron Hydrochloride
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA090817
Rev. Date: 


Appearance:


Markings: T;G1
Shapes:  Round
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.

T G1: (51672-4138) Granisetron 1 mg (Granisetron Hydrochloride 1.12 mg) Oral Tablet by Taro Pharmaceuticals U.S.a., 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:

  • 51672-4138-0: 100 BLISTER PACK IN 1 CARTON (51672‑4138‑0) > 1 TABLET, FILM COATED IN 1 BLISTER PACK
  • 51672-4138-1: 100 TABLET, FILM COATED IN 1 BOTTLE (51672‑4138‑1)
  • 51672-4138-6: 20 TABLET, FILM COATED IN 1 BOTTLE (51672‑4138‑6)

Active Ingredients:

  • Granisetron Hydrochloride

Dosage Strength:

  • 1.12 mg

Inactive Ingredients:

  • Lactose Monohydrate
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Hypromellose
  • Polyethylene Glycol
  • Polysorbate 80
  • 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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