0002-1975 : Axiron 30 mg/1.5ml Topical Solution


NDC0002-1975
Labeler: Eli Lilly and Company
Product Type: Human Prescription Drug
Drug Name:  Axiron
Dosage Form: Topical Solution
Application #: NDA022504
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:

  • 0002-1975-61: 1 BOTTLE, WITH APPLICATOR IN 1 CARTON (0002‑1975‑61) > 90 ML IN 1 BOTTLE, WITH APPLICATOR
  • 0002-1975-90: 1 BOTTLE, WITH APPLICATOR IN 1 CARTON (0002‑1975‑90) > 90 ML IN 1 BOTTLE, WITH APPLICATOR

Active Ingredients:

  • Testosterone

Dosage Strength:

  • 30 mg/1.5mL

Pharmaceutical Classes:

  • Androgen [EPC]
  • Androgen Receptor Agonists [MoA]
  • Androstanes [Chemical/Ingredient]

Related Products:

Based on records with the same trade name.
  • 0002-1977 Axiron 30 mg/1.5ml Topical Solution by Eli Lilly and Company
  • 54868-6406 Axiron 30 mg/1.5ml Topical Solution by Physicians Total Care, Inc.

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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.