Reserpine - 0185-0032-01 - (Reserpine)

Alphabetical Index


Drug Information of Reserpine

Product NDC: 0185-0032
Proprietary Name: Reserpine
Non Proprietary Name: Reserpine
Active Ingredient(s): .1    mg/1 & nbsp;   Reserpine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Reserpine

Product NDC: 0185-0032
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA009838
Marketing Category: NDA
Start Marketing Date: 19880311

Package Information of Reserpine

Package NDC: 0185-0032-01
Package Description: 100 TABLET in 1 BOTTLE (0185-0032-01)

NDC Information of Reserpine

NDC Code 0185-0032-01
Proprietary Name Reserpine
Package Description 100 TABLET in 1 BOTTLE (0185-0032-01)
Product NDC 0185-0032
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Reserpine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19880311
Marketing Category Name NDA
Labeler Name Eon Labs, Inc.
Substance Name RESERPINE
Strength Number .1
Strength Unit mg/1
Pharmaceutical Classes Catecholamine-depleting Sympatholytic [EPC],Decreased Sympathetic Activity [PE]

Complete Information of Reserpine


General Information