Package 72162-2256-1
Brand: doxycycline hyclate
Generic: doxycycline hyclatePackage Facts
Identity
Package NDC
72162-2256-1
Digits Only
7216222561
Product NDC
72162-2256
Description
100 TABLET in 1 BOTTLE (72162-2256-1)
Marketing
Marketing Status
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": "c3d3fe43-2edf-485c-8cdc-3ca5970c0693", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["283535"], "spl_set_id": ["861b71f3-37e8-4596-838c-c8dad8ed5ff4"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2256-1)", "package_ndc": "72162-2256-1", "marketing_start_date": "20190830"}], "brand_name": "Doxycycline Hyclate", "product_id": "72162-2256_c3d3fe43-2edf-485c-8cdc-3ca5970c0693", "dosage_form": "TABLET", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72162-2256", "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": "20 mg/1"}], "application_number": "ANDA065182", "marketing_category": "ANDA", "marketing_start_date": "20190830", "listing_expiration_date": "20261231"}