Package 72266-237-05
Brand: doxycycline
Generic: doxycyclinePackage Facts
Identity
Package NDC
72266-237-05
Digits Only
7226623705
Product NDC
72266-237
Description
5 VIAL in 1 CARTON (72266-237-05) / 10 mL in 1 VIAL (72266-237-01)
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": ["INTRAVENOUS"], "spl_id": "31ba285b-5aef-ff76-e063-6294a90a9321", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["310027"], "spl_set_id": ["fa3fbb09-b830-60c5-e053-6394a90a4165"], "manufacturer_name": ["FOSUN PHARMA USA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL in 1 CARTON (72266-237-05) / 10 mL in 1 VIAL (72266-237-01)", "package_ndc": "72266-237-05", "marketing_start_date": "20230412"}], "brand_name": "DOXYCYCLINE", "product_id": "72266-237_31ba285b-5aef-ff76-e063-6294a90a9321", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72266-237", "generic_name": "DOXYCYCLINE", "labeler_name": "FOSUN PHARMA USA INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/10mL"}], "application_number": "ANDA215583", "marketing_category": "ANDA", "marketing_start_date": "20230412", "listing_expiration_date": "20261231"}