Package 68071-3340-4

Brand: alendronate sodium

Generic: alendronate sodium
NDC Package

Package Facts

Identity

Package NDC 68071-3340-4
Digits Only 6807133404
Product NDC 68071-3340
Product ID 68071-3340_1cd71696-d95a-be3e-e063-6394a90a28c8
Description

4 TABLET in 1 BOX (68071-3340-4)

Marketing

Marketing Status
Marketed Since 2017-07-21
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": "1cd71696-d95a-be3e-e063-6394a90a28c8", "openfda": {"upc": ["0368071334043"], "unii": ["2UY4M2U3RA"], "rxcui": ["904431"], "spl_set_id": ["54d6543d-4239-58b1-e054-00144ff88e88"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BOX (68071-3340-4)", "package_ndc": "68071-3340-4", "marketing_start_date": "20170721"}], "brand_name": "ALENDRONATE SODIUM", "product_id": "68071-3340_1cd71696-d95a-be3e-e063-6394a90a28c8", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "68071-3340", "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"}