Package 70710-1124-3

Brand: doxycycline

Generic: doxycycline
NDC Package

Package Facts

Identity

Package NDC 70710-1124-3
Digits Only 7071011243
Product NDC 70710-1124
Product ID 70710-1124_24db9fe2-5c05-42d0-b113-307484699e9a
Description

30 TABLET, FILM COATED in 1 BOTTLE (70710-1124-3)

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": "24db9fe2-5c05-42d0-b113-307484699e9a", "openfda": {"nui": ["N0000175882", "N0000007948"], "unii": ["N12000U13O"], "rxcui": ["1649429", "1650142", "1650444", "1652673"], "spl_set_id": ["bc321932-b600-4659-a499-1853991b4ab9"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70710-1124-1)", "package_ndc": "70710-1124-1", "marketing_start_date": "20180111"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70710-1124-3)", "package_ndc": "70710-1124-3", "marketing_start_date": "20180111"}], "brand_name": "Doxycycline", "product_id": "70710-1124_24db9fe2-5c05-42d0-b113-307484699e9a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70710-1124", "generic_name": "Doxycycline", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "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"}