52427-803 : Gralise 300 mg Oral Tablet, Film Coated


NDC: 52427-803
Labeler: Almatica Pharma LLC
Product Type: Human Prescription Drug
Drug Name:  Gralise
Dosage Form: Oral Tablet, Film Coated
Application #: NDA022544
Rev. Date: 


NDC Package Codes:

  • 52427-803-90: 90 TABLET, FILM COATED IN 1 BOTTLE (52427‑803‑90)

Active Ingredients:

  • Gabapentin

Dosage Strength:

  • 300 mg

Pharmaceutical Classes:

  • Anti-epileptic Agent [EPC]
  • Decreased Central Nervous System Disorganized Electrical Activity [PE]

Related Products:

Based on records with the same trade name.
  • 52427-804 Gralise 450 mg Oral Tablet, Film Coated by Almatica Pharma LLC
  • 52427-806 Gralise 600 mg Oral Tablet, Film Coated by Almatica Pharma LLC
  • 52427-815 GraliseGralise Kit by Almatica Pharma LLC
  • 52427-850 Gralise 750 mg Oral Tablet, Film Coated by Almatica Pharma LLC
  • 52427-890 Gralise 900 mg Oral Tablet, Film Coated by Almatica Pharma LLC
  • 13913-004 Gralise 300 mg Oral Tablet by Depomed, Inc.
  • 13913-005 Gralise 600 mg Oral Tablet by Depomed, Inc.
  • 13913-006 Gralise Starter Pack by Depomed, Inc.
  • 50436-1262 Gralise 600 mg Oral Tablet, Film Coated by Unit Dose Services
  • 63629-5052 Gralise 600 mg Oral Tablet, Film Coated by Bryant Ranch Prepack

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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.