NDC 68071-4702 Mefloquine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68071 - Nucare Pharmaceuticals,inc.
- 68071-4702 - Mefloquine Hydrochloride
Product Characteristics
Product Packages
NDC Code 68071-4702-8
Package Description: 1 TABLET in 1 BOTTLE
Product Details
What is NDC 68071-4702?
What are the uses for Mefloquine Hydrochloride?
Which are Mefloquine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- MEFLOQUINE HYDROCHLORIDE (UNII: 5Y9L3636O3)
- MEFLOQUINE (UNII: TML814419R) (Active Moiety)
Which are Mefloquine 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STARCH, CORN (UNII: O8232NY3SJ)
- CROSPOVIDONE (15 MPA.S AT 5%) (UNII: 68401960MK)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLOXAMER 188 (UNII: LQA7B6G8JG)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Mefloquine Hydrochloride?
- RxCUI: 835913 - mefloquine HCl 250 MG Oral Tablet
- RxCUI: 835913 - mefloquine hydrochloride 250 MG Oral Tablet
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Patient Education
Mefloquine
Mefloquine is used to treat malaria (a serious infection that is spread by mosquitoes in certain parts of the world and can cause death) and to prevent malaria in travelers who visit areas where malaria is common. Mefloquine is in a class of medications called antimalarials. It works by killing the organisms that cause malaria.
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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".