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Potassium Bicarbonate - 0245-0039-30 - (Potassium Bicarbonate)

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Drug Information of Potassium Bicarbonate

Product NDC: 0245-0039
Proprietary Name: Potassium Bicarbonate
Non Proprietary Name: Potassium Bicarbonate
Active Ingredient(s): 2.5    g/1 & nbsp;   Potassium Bicarbonate
Administration Route(s): ORAL
Dosage Form(s): TABLET, EFFERVESCENT
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Bicarbonate

Product NDC: 0245-0039
Labeler Name: Upsher-Smith Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20021201

Package Information of Potassium Bicarbonate

Package NDC: 0245-0039-30
Package Description: 30 TABLET, EFFERVESCENT in 1 CARTON (0245-0039-30)

NDC Information of Potassium Bicarbonate

NDC Code 0245-0039-30
Proprietary Name Potassium Bicarbonate
Package Description 30 TABLET, EFFERVESCENT in 1 CARTON (0245-0039-30)
Product NDC 0245-0039
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Bicarbonate
Dosage Form Name TABLET, EFFERVESCENT
Route Name ORAL
Start Marketing Date 20021201
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Upsher-Smith Laboratories, Inc.
Substance Name POTASSIUM BICARBONATE
Strength Number 2.5
Strength Unit g/1
Pharmaceutical Classes

Complete Information of Potassium Bicarbonate


General Information