Package 62135-623-90
Brand: doxycycline hyclate
Generic: doxycycline hyclatePackage Facts
Identity
Package NDC
62135-623-90
Digits Only
6213562390
Product NDC
62135-623
Description
90 TABLET, FILM COATED in 1 BOTTLE (62135-623-90)
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": "32d032a2-c17d-4b61-e063-6394a90a9a95", "openfda": {"upc": ["0362135623906"], "unii": ["19XTS3T51U"], "rxcui": ["283535"], "spl_set_id": ["b3294889-e8f8-42f1-9bd0-13d87572997a"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62135-623-90)", "package_ndc": "62135-623-90", "marketing_start_date": "20230220"}], "brand_name": "Doxycycline Hyclate", "product_id": "62135-623_32d032a2-c17d-4b61-e063-6394a90a9a95", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "62135-623", "generic_name": "Doxycycline Hyclate", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "20 mg/1"}], "application_number": "ANDA065277", "marketing_category": "ANDA", "marketing_start_date": "20051110", "listing_expiration_date": "20261231"}