Package 67296-2075-2

Brand: doxycycline hyclate

Generic: doxycycline hyclate
NDC Package

Package Facts

Identity

Package NDC 67296-2075-2
Digits Only 6729620752
Product NDC 67296-2075
Product ID 67296-2075_2c641265-66df-dc3f-e063-6394a90a5a55
Description

20 TABLET in 1 BOTTLE (67296-2075-2)

Marketing

Marketing Status
Marketed Since 2022-02-14
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": "2c641265-66df-dc3f-e063-6394a90a5a55", "openfda": {"upc": ["0327808234018", "0327808234025"], "unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["0b251a58-30d8-dfec-e063-6294a90a3b45"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (67296-2075-2)", "package_ndc": "67296-2075-2", "marketing_start_date": "20220214"}], "brand_name": "DOXYCYCLINE HYCLATE", "product_id": "67296-2075_2c641265-66df-dc3f-e063-6394a90a5a55", "dosage_form": "TABLET", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "67296-2075", "generic_name": "DOXYCYCLINE HYCLATE", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE HYCLATE", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA211343", "marketing_category": "ANDA", "marketing_start_date": "20191009", "listing_expiration_date": "20261231"}