66887-001 : Testim 50 mg/5g Transdermal Gel


NDC: 66887-001
Labeler: Auxilium Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name:  Testim
Dosage Form: Transdermal Gel
Application #: NDA021454
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.

NDC Package Codes:

  • 66887-001-05: 30 TUBE IN 1 CARTON (66887‑001‑05) > 5 G IN 1 TUBE

Active Ingredients:

  • Testosterone

Dosage Strength:

  • 50 mg/5g

Pharmaceutical Classes:

  • Androgen Receptor Agonists [MoA]
  • Androgen [EPC]
  • Androstanes [CS]

Related Products:

Based on records with the same trade name.
  • 16590-853 Testim 50 mg/5g Topical Gel by Stat Rx USA
  • 35356-758 Testim 50 mg/5g Transdermal Gel by Lake Erie Medical Dba Quality Care Products LLC
  • 50090-0875 Testim 50 mg/5g Transdermal Gel by A-s Medication Solutions LLC
  • 54569-5595 Testim 50 mg/5g Transdermal Gel by A-s Medication Solutions LLC
  • 54868-4989 Testim 50 mg/5g Transdermal Gel by Physicians Total Care, Inc.

NDC QR Code

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NDC 66887-001 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.