13913-005 : Gralise 600 mg Oral Tablet


NDC: 13913-005
Labeler: Depomed, Inc.
Product Type: Human Prescription Drug
Drug Name:  Gralise
Dosage Form: Oral Tablet, Film Coated
Application #: NDA022544
Rev. Date: 


Appearance:


Markings: SLV;600
Shapes:  Oval
Colors:  Brown
Size (mm): 19
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.

SLV 600: (13913-005) Gralise 600 mg Oral Tablet by Depomed, 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:

  • 13913-005-19: 90 TABLET, FILM COATED IN 1 BOTTLE (13913‑005‑19)

Active Ingredients:

  • Gabapentin

Dosage Strength:

  • 600 mg

Inactive Ingredients:

  • Copovidone
  • Hypromelloses
  • Magnesium Stearate
  • Polyethylene Glycols
  • Polyvinyl Alcohol
  • Titanium Dioxide
  • Talc
  • Polyethylene Glycol 3350
  • Ferric Oxide Yellow
  • Ferric Oxide Red

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 13913-004 Gralise 300 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
  • 52427-803 Gralise 300 mg Oral Tablet, Film Coated by Almatica Pharma LLC
  • 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
  • 63629-5052 Gralise 600 mg Oral Tablet, Film Coated by Bryant Ranch Prepack

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 13913-005 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.