NDC 79739-7183 Mecamylamine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 79739 - Lgm Pharma Solutions, Llc
- 79739-7183 - Mecamylamine Hydrochloride
Product Characteristics
Product Packages
NDC Code 79739-7183-1
Package Description: 100 TABLET in 1 BOTTLE
Product Details
What is NDC 79739-7183?
What are the uses for Mecamylamine Hydrochloride?
Which are Mecamylamine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- MECAMYLAMINE HYDROCHLORIDE (UNII: 4956DJR58O)
- MECAMYLAMINE (UNII: 6EE945D3OK) (Active Moiety)
Which are Mecamylamine Hydrochloride 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
- STARCH, CORN (UNII: O8232NY3SJ)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- TALC (UNII: 7SEV7J4R1U)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Mecamylamine Hydrochloride?
- RxCUI: 1298874 - mecamylamine HCl 2.5 MG Oral Tablet
- RxCUI: 1298874 - mecamylamine hydrochloride 2.5 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".