Package 51655-350-20

Brand: doxycycline

Generic: doxycycline
NDC Package

Package Facts

Identity

Package NDC 51655-350-20
Digits Only 5165535020
Product NDC 51655-350
Description

20 TABLET in 1 BOTTLE, PLASTIC (51655-350-20)

Marketing

Marketing Status
Marketed Since 2022-11-29
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": "49d7ff1e-293a-4374-e063-6394a90aad44", "openfda": {"nui": ["N0000175882", "N0000007948"], "unii": ["N12000U13O"], "rxcui": ["1650142"], "spl_set_id": ["f2f1ee15-9323-1263-e053-2995a90a01fa"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (51655-350-20)", "package_ndc": "51655-350-20", "marketing_start_date": "20221129"}], "brand_name": "Doxycycline", "product_id": "51655-350_49d7ff1e-293a-4374-e063-6394a90aad44", "dosage_form": "TABLET", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "51655-350", "generic_name": "Doxycycline", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "100 mg/1"}], "application_number": "ANDA091605", "marketing_category": "ANDA", "marketing_start_date": "20221129", "listing_expiration_date": "20271231"}