Package 68071-3771-5

Brand: alendronate sodium

Generic: alendronate sodium
NDC Package

Package Facts

Identity

Package NDC 68071-3771-5
Digits Only 6807137715
Product NDC 68071-3771
Product ID 68071-3771_2bade79f-52fa-d5c1-e063-6294a90aa204
Description

15 BLISTER PACK in 1 CARTON (68071-3771-5) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-01-14
Brand alendronate sodium
Generic alendronate sodium
Sample Package No

Linked Drug Pages (1)

ALENDRONATE SODIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2bade79f-52fa-d5c1-e063-6294a90aa204", "openfda": {"upc": ["0368071377156"], "unii": ["2UY4M2U3RA"], "rxcui": ["904431"], "spl_set_id": ["2baf8516-4148-9007-e063-6394a90a8094"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "15 BLISTER PACK in 1 CARTON (68071-3771-5)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "68071-3771-5", "marketing_start_date": "20250114"}], "brand_name": "ALENDRONATE SODIUM", "product_id": "68071-3771_2bade79f-52fa-d5c1-e063-6294a90aa204", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "68071-3771", "generic_name": "Alendronate sodium", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALENDRONATE SODIUM", "active_ingredients": [{"name": "ALENDRONATE SODIUM", "strength": "70 mg/1"}], "application_number": "ANDA076768", "marketing_category": "ANDA", "marketing_start_date": "20080804", "listing_expiration_date": "20261231"}