Loxapine - 51079-903-20 - (loxapine)

Alphabetical Index


Drug Information of Loxapine

Product NDC: 51079-903
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: 51079-903
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076762
Marketing Category: ANDA
Start Marketing Date: 20110809

Package Information of Loxapine

Package NDC: 51079-903-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-903-20) > 1 CAPSULE in 1 BLISTER PACK (51079-903-01)

NDC Information of Loxapine

NDC Code 51079-903-20
Proprietary Name Loxapine
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-903-20) > 1 CAPSULE in 1 BLISTER PACK (51079-903-01)
Product NDC 51079-903
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name loxapine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110809
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
Substance Name LOXAPINE SUCCINATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loxapine


General Information