55513-369 : OtezlaOtezla Kit


NDC55513-369
Labeler: Amgen Inc
Product Type: Human Prescription Drug
Drug Name:  Otezla
Dosage Form: Kit
Application #: NDA205437
Rev. Date: 


Appearance:


Markings: APR;10
APR;20
APR;30
Shapes:  Diamond (4 sides)
Colors:  White
Pink
Brown
Size (mm): 10
12
8
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:

  • 55513-369-55: 1 BLISTER PACK IN 1 CARTON (55513‑369‑55) > 1 KIT IN 1 BLISTER PACK

Active Ingredients:

  • Apremilast

Kit Contents:

  • Otezla

Inactive Ingredients:

  • Lactose Monohydrate
  • Microcrystalline Cellulose
  • Croscarmellose Sodium
  • Magnesium Stearate
  • Polyvinyl Alcohol, Unspecified
  • Titanium Dioxide
  • Polyethylene Glycol, Unspecified
  • Talc
  • Ferric Oxide Red /
  • Lactose Monohydrate
  • Microcrystalline Cellulose
  • Croscarmellose Sodium
  • Magnesium Stearate
  • Polyvinyl Alcohol, Unspecified
  • Titanium Dioxide
  • Polyethylene Glycol, Unspecified
  • Talc
  • Ferric Oxide Red
  • Ferric Oxide Yellow /
  • Lactose Monohydrate
  • Microcrystalline Cellulose
  • Croscarmellose Sodium
  • Magnesium Stearate
  • Polyvinyl Alcohol, Unspecified
  • Titanium Dioxide
  • Polyethylene Glycol, Unspecified
  • Talc
  • Ferric Oxide Red
  • Ferric Oxide Yellow
  • Ferrosoferric Oxide /

Related Products:

Based on records with the same trade name.
  • 55513-137 Otezla 30 mg Oral Tablet, Film Coated by Amgen Inc
  • 55513-485 OtezlaOtezla Kit by Amgen Inc
  • 55513-497 Otezla 20 mg Oral Tablet, Film Coated by Amgen Inc
  • 55513-508 OtezlaOtezla Kit by Amgen Inc
  • 55513-996 OtezlaOtezla Kit by Amgen Inc
  • 59572-630 Otezla Oral Kit by Celgene Corporation
  • 59572-631 Otezla 30 mg Oral Tablet, Film Coated by Celgene Corporation
  • 59572-632 Otezla Oral Kit by Celgene Corporation
  • 70518-3155 Otezla 30 mg Oral Tablet, Film Coated by Remedyrepack Inc.

NDC QR Code

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NDC 55513-369 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.