Loxapine - 0378-7010-01 - (loxapine)

Alphabetical Index


Drug Information of Loxapine

Product NDC: 0378-7010
Proprietary Name: Loxapine
Non Proprietary Name: loxapine
Active Ingredient(s): 10    mg/1 & nbsp;   loxapine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Loxapine

Product NDC: 0378-7010
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076762
Marketing Category: ANDA
Start Marketing Date: 20121105

Package Information of Loxapine

Package NDC: 0378-7010-01
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-7010-01)

NDC Information of Loxapine

NDC Code 0378-7010-01
Proprietary Name Loxapine
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-7010-01)
Product NDC 0378-7010
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name loxapine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20121105
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name LOXAPINE SUCCINATE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loxapine


General Information