Package 0591-4550-22

Brand: doxycycline hyclate

Generic: doxycycline hyclate
NDC Package

Package Facts

Identity

Package NDC 0591-4550-22
Digits Only 0591455022
Product NDC 0591-4550
Product ID 0591-4550_d2422c7a-2c5f-4377-8828-2f53f09a7246
Description

120 TABLET, DELAYED RELEASE in 1 BOTTLE (0591-4550-22)

Marketing

Marketing Status
Marketed Since 2019-08-14
Brand doxycycline hyclate
Generic doxycycline hyclate
Sample Package No

Linked Drug Pages (1)

Doxycycline Hyclate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d2422c7a-2c5f-4377-8828-2f53f09a7246", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1423080", "1653433"], "spl_set_id": ["c2b08332-3256-4658-965a-ede3d973a388"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE (0591-4550-22)", "package_ndc": "0591-4550-22", "marketing_start_date": "20190814"}], "brand_name": "Doxycycline Hyclate", "product_id": "0591-4550_d2422c7a-2c5f-4377-8828-2f53f09a7246", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "0591-4550", "generic_name": "Doxycycline Hyclate", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "50 mg/1"}], "application_number": "ANDA090134", "marketing_category": "ANDA", "marketing_start_date": "20190814", "listing_expiration_date": "20261231"}