Package 42708-173-20

Brand: doxycycline hyclate

Generic: doxycycline hyclate
NDC Package Sample

Package Facts

Identity

Package NDC 42708-173-20
Digits Only 4270817320
Product NDC 42708-173
Description

20 TABLET, COATED in 1 BOTTLE, PLASTIC (42708-173-20)

Marketing

Marketing Status
Marketed Since 2023-05-19
Brand doxycycline hyclate
Generic doxycycline hyclate
Sample Package Yes

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46827da0-577c-60e7-e063-6294a90a99e7", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["fbd0a22f-b365-c0a2-e053-6394a90a1e07"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "20 TABLET, COATED in 1 BOTTLE, PLASTIC (42708-173-20)", "package_ndc": "42708-173-20", "marketing_start_date": "20230519"}], "brand_name": "Doxycycline Hyclate", "product_id": "42708-173_46827da0-577c-60e7-e063-6294a90a99e7", "dosage_form": "TABLET, COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "42708-173", "generic_name": "Doxycycline Hyclate", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA065095", "marketing_category": "ANDA", "marketing_start_date": "20030702", "listing_expiration_date": "20261231"}