0009-0019 : Halotestin 5 mg Oral Tablet


NDC: 0009-0019
Labeler: Pharmacia and Upjohn Company
Drug Name:  Halotestin
Rev. Date: 
CSA Schedule: CIII (US) [1]


[1] Schedule III / IIIN Controlled Substance: Has a potential for abuse less than substances in Schedules I or II and abuse may lead to moderate or low physical dependence or high psychological dependence. (i.e. Products containing not more than 90 milligrams of Codeine per dosage unit [such as Tylenol with Codeine], other narcotics such as Buprenorphine (Suboxone), and Schedule IIIN non-narcotics such as Didrex, Ketamine, Phendimetrazine, and Anabolic Steroids). More Details: US Dept of Justice Controlled Substance Schedules.

Appearance:


Markings: HALOTESTIN;5
Shapes:  Round
Colors:  Green
Size (mm): 7
Segments: * 2

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces.

Active Ingredients:

  • Fluoxymesterone

Inactive Ingredients:

  • Calcium Stearate
  • Corn Starch
  • Fd&c Yellow No. 5
  • Lactose
  • Sorbic Acid
  • Sucrose
  • Tragacanth
  • Fd&c Blue No. 2

Related Products:

Based on records with the same trade name.
  • 0009-0014 Halotestin 2 mg Oral Tablet by Pharmacia and Upjohn Company
  • 0009-0036 Halotestin 10 mg Oral Tablet by Pharmacia and Upjohn Company

NDC QR Code

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NDC 0009-0019 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.