Home > National Drug Code (NDC) > Pravastatin sodium

Pravastatin sodium - 55111-230-01 - (Pravastatin sodium)

Alphabetical Index


Drug Information of Pravastatin sodium

Product NDC: 55111-230
Proprietary Name: Pravastatin sodium
Non Proprietary Name: Pravastatin sodium
Active Ingredient(s): 20    mg/1 & nbsp;   Pravastatin sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Pravastatin sodium

Product NDC: 55111-230
Labeler Name: Dr.Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076714
Marketing Category: ANDA
Start Marketing Date: 20091231

Package Information of Pravastatin sodium

Package NDC: 55111-230-01
Package Description: 100 TABLET in 1 BOTTLE (55111-230-01)

NDC Information of Pravastatin sodium

NDC Code 55111-230-01
Proprietary Name Pravastatin sodium
Package Description 100 TABLET in 1 BOTTLE (55111-230-01)
Product NDC 55111-230
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pravastatin sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091231
Marketing Category Name ANDA
Labeler Name Dr.Reddy's Laboratories Limited
Substance Name PRAVASTATIN SODIUM
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Complete Information of Pravastatin sodium


General Information