Package 70518-3214-0

Brand: doxycycline hyclate

Generic: doxycycline hyclate
NDC Package

Package Facts

Identity

Package NDC 70518-3214-0
Digits Only 7051832140
Product NDC 70518-3214
Description

14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3214-0)

Marketing

Marketing Status
Marketed Since 2021-09-08
Brand doxycycline hyclate
Generic doxycycline hyclate
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a3470c0-261d-4741-e063-6294a90a47c0", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["2305ab4a-7d08-41f6-9c39-c9b6835be389"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3214-0)", "package_ndc": "70518-3214-0", "marketing_start_date": "20210908"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3214-5)", "package_ndc": "70518-3214-5", "marketing_start_date": "20250130"}], "brand_name": "Doxycycline Hyclate", "product_id": "70518-3214_3a3470c0-261d-4741-e063-6294a90a47c0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70518-3214", "generic_name": "Doxycycline Hyclate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA062269", "marketing_category": "ANDA", "marketing_start_date": "20210908", "listing_expiration_date": "20261231"}