Loxapine - 0527-1397-01 - (Loxapine)

Alphabetical Index


Drug Information of Loxapine

Product NDC: 0527-1397
Proprietary Name: Loxapine
Non Proprietary Name: Loxapine
Active Ingredient(s): 50    mg/1 & nbsp;   Loxapine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Loxapine

Product NDC: 0527-1397
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090695
Marketing Category: ANDA
Start Marketing Date: 20110926

Package Information of Loxapine

Package NDC: 0527-1397-01
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (0527-1397-01)

NDC Information of Loxapine

NDC Code 0527-1397-01
Proprietary Name Loxapine
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (0527-1397-01)
Product NDC 0527-1397
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Loxapine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110926
Marketing Category Name ANDA
Labeler Name Lannett Company, Inc.
Substance Name LOXAPINE SUCCINATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loxapine


General Information