16729-273 : Prasugrel 10 mg Oral Tablet, Film Coated


NDC: 16729-273
Labeler: Accord Healthcare Inc.
Product Type: Human Prescription Drug
Drug Name:  Prasugrel
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA205987
Rev. Date: 


Appearance:


Markings: AA2
Shapes:  Hexagon (6 sides)
Colors:  Brown
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:

  • 16729-273-10: 30 TABLET, FILM COATED IN 1 BOTTLE (16729‑273‑10)

Active Ingredients:

  • Prasugrel Hydrochloride

Dosage Strength:

  • 10 mg

Inactive Ingredients:

  • Cellulose, Microcrystalline
  • Hypromellose 2910 (6 Mpa.s)
  • Low-substituted Hydroxypropyl Cellulose (8% Hydroxypropyl: 140000 Mw)
  • Sucrose Stearate
  • Lactose Monohydrate
  • Titanium Dioxide
  • Triacetin
  • Ferric Oxide Yellow
  • Ferric Oxide Red
  • Hypromellose 2910 (5 Mpa.s) /

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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  • 51407-444 Prasugrel 5 mg Oral Tablet, Film Coated by Golden State Medical Supply, Inc.
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  • 60505-4642 Prasugrel 5 mg Oral Tablet, Film Coated by Apotex Corp.
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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.