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Mefloquine Hydrochloride - 21695-449-07 - (Mefloquine Hydrochloride)

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Drug Information of Mefloquine Hydrochloride

Product NDC: 21695-449
Proprietary Name: Mefloquine Hydrochloride
Non Proprietary Name: Mefloquine Hydrochloride
Active Ingredient(s): 250    mg/1 & nbsp;   Mefloquine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Mefloquine Hydrochloride

Product NDC: 21695-449
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076392
Marketing Category: ANDA
Start Marketing Date: 20031229

Package Information of Mefloquine Hydrochloride

Package NDC: 21695-449-07
Package Description: 7 TABLET in 1 BOTTLE (21695-449-07)

NDC Information of Mefloquine Hydrochloride

NDC Code 21695-449-07
Proprietary Name Mefloquine Hydrochloride
Package Description 7 TABLET in 1 BOTTLE (21695-449-07)
Product NDC 21695-449
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mefloquine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20031229
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name MEFLOQUINE HYDROCHLORIDE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Antimalarial [EPC]

Complete Information of Mefloquine Hydrochloride


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