NDC 0115-7037 Methitest
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0115 - Amneal Pharmaceuticals Of New York Llc
- 0115-7037 - Methitest
Product Characteristics
Product Packages
NDC Code 0115-7037-01
Package Description: 100 TABLET in 1 BOTTLE
Product Details
What is NDC 0115-7037?
What are the uses for Methitest?
Which are Methitest UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYLTESTOSTERONE (UNII: V9EFU16ZIF)
- METHYLTESTOSTERONE (UNII: V9EFU16ZIF) (Active Moiety)
Which are Methitest Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- ACACIA (UNII: 5C5403N26O)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- SUCROSE (UNII: C151H8M554)
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- GUAR GUM (UNII: E89I1637KE)
What is the NDC to RxNorm Crosswalk for Methitest?
- RxCUI: 197976 - methylTESTOSTERone 10 MG Oral Tablet
- RxCUI: 197976 - methyltestosterone 10 MG Oral Tablet
- RxCUI: 541524 - METHITEST 10 MG Oral Tablet
- RxCUI: 541524 - methyltestosterone 10 MG Oral Tablet [Methitest]
- RxCUI: 541524 - Methitest 10 MG Oral Tablet
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".