Package 72162-2402-2

Brand: doxycycline hyclate

Generic: doxycycline hyclate
NDC Package

Package Facts

Identity

Package NDC 72162-2402-2
Digits Only 7216224022
Product NDC 72162-2402
Description

14 TABLET in 1 BOTTLE (72162-2402-2)

Marketing

Marketing Status
Marketed Since 2024-10-08
Brand doxycycline hyclate
Generic doxycycline hyclate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ffaac40e-5fd1-4115-ab63-cb13723c1f7d", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["fd58dbe5-aab2-4378-b054-d5c60d87074e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE (72162-2402-2)", "package_ndc": "72162-2402-2", "marketing_start_date": "20241008"}], "brand_name": "DOXYCYCLINE HYCLATE", "product_id": "72162-2402_ffaac40e-5fd1-4115-ab63-cb13723c1f7d", "dosage_form": "TABLET", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72162-2402", "generic_name": "DOXYCYCLINE HYCLATE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE HYCLATE", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA211343", "marketing_category": "ANDA", "marketing_start_date": "20191009", "listing_expiration_date": "20261231"}