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POTASSIUM CITRATE - 64980-137-01 - (POTASSIUM CITRATE)

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Drug Information of POTASSIUM CITRATE

Product NDC: 64980-137
Proprietary Name: POTASSIUM CITRATE
Non Proprietary Name: POTASSIUM CITRATE
Active Ingredient(s): 540    mg/1 & nbsp;   POTASSIUM CITRATE
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of POTASSIUM CITRATE

Product NDC: 64980-137
Labeler Name: Rising Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077440
Marketing Category: ANDA
Start Marketing Date: 20060619

Package Information of POTASSIUM CITRATE

Package NDC: 64980-137-01
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (64980-137-01)

NDC Information of POTASSIUM CITRATE

NDC Code 64980-137-01
Proprietary Name POTASSIUM CITRATE
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (64980-137-01)
Product NDC 64980-137
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name POTASSIUM CITRATE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20060619
Marketing Category Name ANDA
Labeler Name Rising Pharmaceuticals, Inc.
Substance Name POTASSIUM CITRATE
Strength Number 540
Strength Unit mg/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of POTASSIUM CITRATE


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