Loxapine - 68084-004-21 - (Loxapine)

Alphabetical Index


Drug Information of Loxapine

Product NDC: 68084-004
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: 68084-004
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090695
Marketing Category: ANDA
Start Marketing Date: 20130624

Package Information of Loxapine

Package NDC: 68084-004-21
Package Description: 3 BLISTER PACK in 1 CARTON (68084-004-21) > 10 CAPSULE in 1 BLISTER PACK (68084-004-11)

NDC Information of Loxapine

NDC Code 68084-004-21
Proprietary Name Loxapine
Package Description 3 BLISTER PACK in 1 CARTON (68084-004-21) > 10 CAPSULE in 1 BLISTER PACK (68084-004-11)
Product NDC 68084-004
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Loxapine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130624
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name LOXAPINE SUCCINATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loxapine


General Information