0115-7037 : Methitest 10 mg Oral Tablet

NDC:	0115-7037
Labeler:	Global Pharmaceuticals, Division of Impax Laboratories Inc.
Product Type:	Human Prescription Drug
Drug Name:	Methitest
Dosage Form:	Oral Tablet
Application #:	ANDA080767
Rev. Date:	Oct 17, 1974
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:	7037
Shapes:	Round
Colors:	White
Size (mm):	10
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.

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:

• 0115-7037-01: 100 TABLET IN 1 BOTTLE (0115‑7037‑01)

Active Ingredients:

• Methyltestosterone

Inactive Ingredients:

• Acacia
• Lactose Monohydrate
• Sucrose
• Starch, Corn
• Sodium Lauryl Sulfate
• Powdered Cellulose
• Magnesium Stearate
• Guar Gum

Pharmaceutical Classes:

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

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