Package 70518-3363-0

Brand: doxycycline

Generic: doxycycline hyclate
NDC Package

Package Facts

Identity

Package NDC 70518-3363-0
Digits Only 7051833630
Product NDC 70518-3363
Description

14 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3363-0)

Marketing

Marketing Status
Marketed Since 2022-02-10
Brand doxycycline
Generic doxycycline hyclate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "497365ff-c7cd-6fd6-e063-6294a90a4d50", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["2c29f716-bdb0-437d-92a4-d856b87db976"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3363-0)", "package_ndc": "70518-3363-0", "marketing_start_date": "20220210"}, {"sample": false, "description": "28 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3363-1)", "package_ndc": "70518-3363-1", "marketing_start_date": "20260127"}], "brand_name": "Doxycycline", "product_id": "70518-3363_497365ff-c7cd-6fd6-e063-6294a90a4d50", "dosage_form": "TABLET, COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70518-3363", "generic_name": "Doxycycline hyclate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA210664", "marketing_category": "ANDA", "marketing_start_date": "20220210", "listing_expiration_date": "20271231"}