Package 0527-1338-50
Brand: doxycycline
Generic: doxycyclinePackage Facts
Identity
Package NDC
0527-1338-50
Digits Only
0527133850
Product NDC
0527-1338
Description
50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1338-50)
Marketing
Marketing Status
Brand
doxycycline
Generic
doxycycline
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "dc960a6c-1b09-4049-a1e9-0109576b1d30", "openfda": {"nui": ["N0000175882", "N0000007948"], "upc": ["0305271537300", "0305271535016"], "unii": ["N12000U13O"], "rxcui": ["1649429", "1650142", "1650444", "1652673"], "spl_set_id": ["4999bbd9-44ed-4749-9730-be2337bdf490"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1338-25)", "package_ndc": "0527-1338-25", "marketing_start_date": "20051208"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1338-50)", "package_ndc": "0527-1338-50", "marketing_start_date": "20051208"}], "brand_name": "Doxycycline", "product_id": "0527-1338_dc960a6c-1b09-4049-a1e9-0109576b1d30", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "0527-1338", "generic_name": "Doxycycline", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "100 mg/1"}], "application_number": "ANDA065285", "marketing_category": "ANDA", "marketing_start_date": "20051208", "listing_expiration_date": "20261231"}