63739-999 : Galantamine 4 mg Oral Tablet, Film Coated


NDC: 63739-999
Labeler: Mckesson Packaging Services a Business Unit of Mckesson Corporation
Product Type: Human Prescription Drug
Drug Name:  Galantamine
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA090957
Rev. Date: 


Appearance:


Markings: F;49
Shapes:  Round
Colors:  White
Size (mm): 5
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.

F 49: (68084-729) Galantamine 4 mg Oral Tablet, Film Coated by Mckesson Packaging Services a Business Unit of Mckesson Corporation
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:

  • 63739-999-33: 3 BLISTER PACK IN 1 BOX, UNIT‑DOSE (63739‑999‑33) > 10 TABLET, FILM COATED IN 1 BLISTER PACK

Active Ingredients:

  • Galantamine Hydrobromide

Dosage Strength:

  • 4 mg

Inactive Ingredients:

  • Silicon Dioxide
  • Hypromellose 2910 (5 Mpa.s)
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Starch, Corn
  • Propylene Glycol
  • Talc
  • Titanium Dioxide
  • Ferric Oxide Yellow

Pharmaceutical Classes:

  • Cholinesterase Inhibitor [EPC]
  • Cholinesterase Inhibitors [MoA]

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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.