Package 24658-711-48

Brand: demeclocycline hydrochloride

Generic: demeclocycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 24658-711-48
Digits Only 2465871148
Product NDC 24658-711
Product ID 24658-711_aa40e353-18db-4553-8f8d-a434eac8ed1f
Description

48 TABLET, FILM COATED in 1 BOTTLE (24658-711-48)

Marketing

Marketing Status
Marketed Since 2017-10-07
Brand demeclocycline hydrochloride
Generic demeclocycline hydrochloride
Sample Package No

Linked Drug Pages (1)

Demeclocycline Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "aa40e353-18db-4553-8f8d-a434eac8ed1f", "openfda": {"upc": ["0324658711485", "0324658710013"], "unii": ["29O079NTYT"], "rxcui": ["905341", "905347"], "spl_set_id": ["88e03cb0-25f5-41a5-b77f-58ab8f3be181"], "manufacturer_name": ["PuraCap Laboratories LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "48 TABLET, FILM COATED in 1 BOTTLE (24658-711-48)", "package_ndc": "24658-711-48", "marketing_start_date": "20171007"}], "brand_name": "Demeclocycline Hydrochloride", "product_id": "24658-711_aa40e353-18db-4553-8f8d-a434eac8ed1f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Antimicrobial [EPC]", "Tetracyclines [CS]"], "product_ndc": "24658-711", "generic_name": "Demeclocycline Hydrochloride", "labeler_name": "PuraCap Laboratories LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Demeclocycline Hydrochloride", "active_ingredients": [{"name": "DEMECLOCYCLINE HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA065447", "marketing_category": "ANDA", "marketing_start_date": "20171007", "listing_expiration_date": "20261231"}