Package 63629-9410-1

Brand: doxycycline

Generic: doxycycline
NDC Package

Package Facts

Identity

Package NDC 63629-9410-1
Digits Only 6362994101
Product NDC 63629-9410
Description

20 TABLET, FILM COATED in 1 BOTTLE (63629-9410-1)

Marketing

Marketing Status
Marketed Since 2024-08-26
Brand doxycycline
Generic doxycycline
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fbac8af2-55e8-4bb5-90f7-4019be864f65", "openfda": {"nui": ["N0000175882", "N0000007948"], "unii": ["N12000U13O"], "rxcui": ["1650142"], "spl_set_id": ["5f22094e-9297-4d1b-a37c-7846481b321e"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (63629-9410-1)", "package_ndc": "63629-9410-1", "marketing_start_date": "20240826"}], "brand_name": "Doxycycline", "product_id": "63629-9410_fbac8af2-55e8-4bb5-90f7-4019be864f65", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "63629-9410", "generic_name": "Doxycycline", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "100 mg/1"}], "application_number": "ANDA065285", "marketing_category": "ANDA", "marketing_start_date": "20051208", "listing_expiration_date": "20261231"}