Potassium Chloride
POTASSIUM CHLORIDE EXTENDED-RELEASE TABLETS, USP
Approved
Approval ID
aa6d9e02-0ff8-421d-9ddd-8968f41f0af7
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 17, 2011
Manufacturers
FDA
Rebel Distributors Corp
DUNS: 118802834
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Potassium Chloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code21695-712
Application NumberANDA075604
Product Classification
M
Marketing Category
C73584
G
Generic Name
Potassium Chloride
Product Specifications
Route of AdministrationORAL
Effective DateNovember 30, 2010
FDA Product Classification
INGREDIENTS (5)
POTASSIUM CHLORIDEActive
Quantity: 20 meq in 1 1
Code: 660YQ98I10
Classification: ACTIB
CROSPOVIDONEInactive
Code: 68401960MK
Classification: IACT
ACETYLTRIBUTYL CITRATEInactive
Code: 0ZBX0N59RZ
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
ETHYLCELLULOSE (10 MPA.S)Inactive
Code: 3DYK7UYZ62
Classification: IACT
Potassium Chloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code21695-711
Application NumberANDA075604
Product Classification
M
Marketing Category
C73584
G
Generic Name
Potassium Chloride
Product Specifications
Route of AdministrationORAL
Effective DateNovember 30, 2010
FDA Product Classification
INGREDIENTS (5)
POTASSIUM CHLORIDEActive
Quantity: 10 meq in 1 1
Code: 660YQ98I10
Classification: ACTIB
CROSPOVIDONEInactive
Code: 68401960MK
Classification: IACT
ETHYLCELLULOSE (10 MPA.S)Inactive
Code: 3DYK7UYZ62
Classification: IACT
ACETYLTRIBUTYL CITRATEInactive
Code: 0ZBX0N59RZ
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT