48792-7822 : Prasugrel 5 mg Oral Tablet, Film Coated


NDC: 48792-7822
Labeler: Sunshine Lake Pharma Co., Ltd.
Product Type: Human Prescription Drug
Drug Name:  Prasugrel
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA206021
Rev. Date: 


Appearance:


Markings: S77
Shapes:  Round
Colors:  Pink
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.

NDC Package Codes:

  • 48792-7822-1: 30 TABLET, FILM COATED IN 1 BOTTLE (48792‑7822‑1)

Active Ingredients:

  • Prasugrel Hydrochloride

Dosage Strength:

  • 5 mg

Inactive Ingredients:

  • Mannitol
  • Hypromellose, Unspecified
  • Low-substituted Hydroxypropyl Cellulose, Unspecified
  • Microcrystalline Cellulose
  • Sucrose Stearate
  • Glyceryl Dibehenate
  • Lactose
  • Titanium Dioxide
  • Triacetin
  • Ferric Oxide Red /

Pharmaceutical Classes:

  • Decreased Platelet Aggregation [PE]
  • P2Y12 Platelet Inhibitor [EPC]
  • P2Y12 Receptor Antagonists [MoA]

Related Products:

Based on records with the same trade name.
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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.