CEENU - 0015-3031-20 - (LOMUSTINE)

Alphabetical Index


Drug Information of CEENU

Product NDC: 0015-3031
Proprietary Name: CEENU
Non Proprietary Name: LOMUSTINE
Active Ingredient(s): 40    mg/1 & nbsp;   LOMUSTINE
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of CEENU

Product NDC: 0015-3031
Labeler Name: E.R. Squibb & Sons, L.L.C.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017588
Marketing Category: NDA
Start Marketing Date: 20081215

Package Information of CEENU

Package NDC: 0015-3031-20
Package Description: 1 BOTTLE in 1 CARTON (0015-3031-20) > 20 CAPSULE, GELATIN COATED in 1 BOTTLE

NDC Information of CEENU

NDC Code 0015-3031-20
Proprietary Name CEENU
Package Description 1 BOTTLE in 1 CARTON (0015-3031-20) > 20 CAPSULE, GELATIN COATED in 1 BOTTLE
Product NDC 0015-3031
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LOMUSTINE
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20081215
Marketing Category Name NDA
Labeler Name E.R. Squibb & Sons, L.L.C.
Substance Name LOMUSTINE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Alkylating Activity [MoA],Alkylating Drug [EPC]

Complete Information of CEENU


General Information