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K-EFFERVESCENT - 0603-4170-16 - (POTASSIUM BICARBONATE)

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Drug Information of K-EFFERVESCENT

Product NDC: 0603-4170
Proprietary Name: K-EFFERVESCENT
Non Proprietary Name: POTASSIUM BICARBONATE
Active Ingredient(s): 25    meq/1 & nbsp;   POTASSIUM BICARBONATE
Administration Route(s): ORAL
Dosage Form(s): TABLET, EFFERVESCENT
Coding System: National Drug Codes(NDC)

Labeler Information of K-EFFERVESCENT

Product NDC: 0603-4170
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20060106

Package Information of K-EFFERVESCENT

Package NDC: 0603-4170-16
Package Description: 30 TABLET, EFFERVESCENT in 1 BOX (0603-4170-16)

NDC Information of K-EFFERVESCENT

NDC Code 0603-4170-16
Proprietary Name K-EFFERVESCENT
Package Description 30 TABLET, EFFERVESCENT in 1 BOX (0603-4170-16)
Product NDC 0603-4170
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name POTASSIUM BICARBONATE
Dosage Form Name TABLET, EFFERVESCENT
Route Name ORAL
Start Marketing Date 20060106
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Qualitest Pharmaceuticals
Substance Name POTASSIUM BICARBONATE
Strength Number 25
Strength Unit meq/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of K-EFFERVESCENT


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