REMERON - 0052-0109-30 - (MIRTAZAPINE)

Alphabetical Index


Drug Information of REMERON

Product NDC: 0052-0109
Proprietary Name: REMERON
Non Proprietary Name: MIRTAZAPINE
Active Ingredient(s): 45    mg/1 & nbsp;   MIRTAZAPINE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of REMERON

Product NDC: 0052-0109
Labeler Name: Organon Pharmaceuticals USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020415
Marketing Category: NDA
Start Marketing Date: 19970311

Package Information of REMERON

Package NDC: 0052-0109-30
Package Description: 1 BOTTLE in 1 CARTON (0052-0109-30) > 30 TABLET, FILM COATED in 1 BOTTLE

NDC Information of REMERON

NDC Code 0052-0109-30
Proprietary Name REMERON
Package Description 1 BOTTLE in 1 CARTON (0052-0109-30) > 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC 0052-0109
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MIRTAZAPINE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19970311
Marketing Category Name NDA
Labeler Name Organon Pharmaceuticals USA
Substance Name MIRTAZAPINE
Strength Number 45
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of REMERON


General Information