Package 70771-1009-1

Brand: doxycycline

Generic: doxycycline
NDC Package

Package Facts

Identity

Package NDC 70771-1009-1
Digits Only 7077110091
Product NDC 70771-1009
Product ID 70771-1009_1f788250-9643-4c64-bb4e-4dfefabb8c01
Description

100 TABLET, FILM COATED in 1 BOTTLE (70771-1009-1)

Marketing

Marketing Status
Marketed Since 2018-01-11
Brand doxycycline
Generic doxycycline
Sample Package No

Linked Drug Pages (1)

Doxycycline ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1f788250-9643-4c64-bb4e-4dfefabb8c01", "openfda": {"nui": ["N0000175882", "N0000007948"], "upc": ["0370710112431"], "unii": ["N12000U13O"], "rxcui": ["1649429", "1650142", "1650444", "1652673"], "spl_set_id": ["c886b2e4-494a-4325-abaf-981fc3d01c66"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70771-1009-1)", "package_ndc": "70771-1009-1", "marketing_start_date": "20180111"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70771-1009-3)", "package_ndc": "70771-1009-3", "marketing_start_date": "20180111"}], "brand_name": "Doxycycline", "product_id": "70771-1009_1f788250-9643-4c64-bb4e-4dfefabb8c01", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70771-1009", "generic_name": "Doxycycline", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "150 mg/1"}], "application_number": "ANDA209582", "marketing_category": "ANDA", "marketing_start_date": "20180111", "listing_expiration_date": "20261231"}