Package 69668-515-30

Brand: doxycycline hyclate

Generic: doxycycline hyclate
NDC Package

Package Facts

Identity

Package NDC 69668-515-30
Digits Only 6966851530
Product NDC 69668-515
Product ID 69668-515_6ce404bd-62b7-4aeb-e053-2a91aa0ade68
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (69668-515-30)

Marketing

Marketing Status
Marketed Since 2018-05-10
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": "6ce404bd-62b7-4aeb-e053-2a91aa0ade68", "openfda": {"upc": ["0369668515302"], "unii": ["19XTS3T51U"], "rxcui": ["799048"], "spl_set_id": ["4fa26176-a730-48ed-9659-e2f64212f418"], "manufacturer_name": ["Sonoma Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (69668-515-30)", "package_ndc": "69668-515-30", "marketing_start_date": "20180510"}], "brand_name": "Doxycycline Hyclate", "product_id": "69668-515_6ce404bd-62b7-4aeb-e053-2a91aa0ade68", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "69668-515", "generic_name": "DOXYCYCLINE HYCLATE", "labeler_name": "Sonoma Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "150 mg/1"}], "application_number": "ANDA207494", "marketing_category": "ANDA", "marketing_start_date": "20161128", "listing_expiration_date": "20261231"}