Package 68308-716-60

Brand: doxycycline hyclate

Generic: doxycycline hyclate
NDC Package

Package Facts

Identity

Package NDC 68308-716-60
Digits Only 6830871660
Product NDC 68308-716
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE (68308-716-60)

Marketing

Marketing Status
Marketed Since 2016-02-01
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": "fe12dd75-ce55-4035-9193-0182bc4f5ba6", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["406524", "434018", "799048", "1423080"], "spl_set_id": ["cd2ab9b8-9619-4199-8a5d-83377b3274d1"], "manufacturer_name": ["Mayne Pharma Commercial LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (68308-716-30)", "package_ndc": "68308-716-30", "marketing_start_date": "20171218"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (68308-716-60)", "package_ndc": "68308-716-60", "marketing_start_date": "20160201"}], "brand_name": "Doxycycline Hyclate", "product_id": "68308-716_fe12dd75-ce55-4035-9193-0182bc4f5ba6", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "68308-716", "generic_name": "Doxycycline Hyclate", "labeler_name": "Mayne Pharma Commercial LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "200 mg/1"}], "application_number": "NDA050795", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20160201", "listing_expiration_date": "20261231"}