Package 71335-2638-1

Brand: doxycycline

Generic: doxycycline
NDC Package

Package Facts

Identity

Package NDC 71335-2638-1
Digits Only 7133526381
Product NDC 71335-2638
Product ID 71335-2638_e57b9621-750a-4d3c-b129-f7b0e1e7677d
Description

20 TABLET, FILM COATED in 1 BOTTLE (71335-2638-1)

Marketing

Marketing Status
Marketed Since 2025-06-02
Brand doxycycline
Generic doxycycline
Sample Package No

Linked Drug Pages (1)

Doxycycline ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e57b9621-750a-4d3c-b129-f7b0e1e7677d", "openfda": {"nui": ["N0000175882", "N0000007948"], "unii": ["N12000U13O"], "rxcui": ["1650142"], "spl_set_id": ["b46208a2-5072-4df5-b2af-379f865545d2"], "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 (71335-2638-1)", "package_ndc": "71335-2638-1", "marketing_start_date": "20250602"}], "brand_name": "Doxycycline", "product_id": "71335-2638_e57b9621-750a-4d3c-b129-f7b0e1e7677d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "71335-2638", "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": "ANDA209582", "marketing_category": "ANDA", "marketing_start_date": "20180111", "listing_expiration_date": "20261231"}