Package 49884-111-74

Brand: alprazolam

Generic: alprazolam
NDC Package

Package Facts

Identity

Package NDC 49884-111-74
Digits Only 4988411174
Product NDC 49884-111
Description

10 BLISTER PACK in 1 CARTON (49884-111-74) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2009-01-09
Brand alprazolam
Generic alprazolam
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fac25045-6d3b-420d-b2c0-f2f211236e15", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["485413", "485414", "485415", "485416"], "spl_set_id": ["ff1630b4-2044-433c-96bc-0bb4ae8d42a0"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (49884-111-74)  / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "49884-111-74", "marketing_start_date": "20090109"}], "brand_name": "Alprazolam", "product_id": "49884-111_fac25045-6d3b-420d-b2c0-f2f211236e15", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "49884-111", "dea_schedule": "CIV", "generic_name": "alprazolam", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".5 mg/1"}], "application_number": "ANDA078088", "marketing_category": "ANDA", "marketing_start_date": "20090109", "listing_expiration_date": "20261231"}