Almacone - 21695-840-12 - (Almacone)

Alphabetical Index


Drug Information of Almacone

Product NDC: 21695-840
Proprietary Name: Almacone
Non Proprietary Name: Almacone
Active Ingredient(s): 200; 200    mg/5mL; mg/5mL & nbsp;   Almacone
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Almacone

Product NDC: 21695-840
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN OTC DRUG
FDA Application Number: part331
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20081111

Package Information of Almacone

Package NDC: 21695-840-12
Package Description: 355 mL in 1 BOTTLE (21695-840-12)

NDC Information of Almacone

NDC Code 21695-840-12
Proprietary Name Almacone
Package Description 355 mL in 1 BOTTLE (21695-840-12)
Product NDC 21695-840
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Almacone
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20081111
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Rebel Distributors Corp
Substance Name ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE
Strength Number 200; 200
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Almacone


General Information