Package 80425-0319-1
Brand: doxycycline monohydrate
Generic: doxycycline monohydratePackage Facts
Identity
Package NDC
80425-0319-1
Digits Only
8042503191
Product NDC
80425-0319
Description
30 TABLET, FILM COATED in 1 BOTTLE (80425-0319-1)
Marketing
Marketing Status
Brand
doxycycline monohydrate
Generic
doxycycline monohydrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a9bf7d3-46da-0dfa-e063-6394a90a76a4", "openfda": {"nui": ["N0000175882", "N0000007948"], "unii": ["N12000U13O"], "rxcui": ["1650142"], "spl_set_id": ["f91373f2-c57b-f1f1-e053-6294a90a7bdd"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0319-1)", "package_ndc": "80425-0319-1", "marketing_start_date": "20230411"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0319-2)", "package_ndc": "80425-0319-2", "marketing_start_date": "20230411"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0319-3)", "package_ndc": "80425-0319-3", "marketing_start_date": "20230411"}], "brand_name": "Doxycycline Monohydrate", "product_id": "80425-0319_2a9bf7d3-46da-0dfa-e063-6394a90a76a4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "80425-0319", "generic_name": "Doxycycline Monohydrate", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Monohydrate", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "100 mg/1"}], "application_number": "ANDA209582", "marketing_category": "ANDA", "marketing_start_date": "20230411", "listing_expiration_date": "20261231"}