Package 70518-0033-0

Brand: alendronate sodium

Generic: alendronate sodium
NDC Package

Package Facts

Identity

Package NDC 70518-0033-0
Digits Only 7051800330
Product NDC 70518-0033
Product ID 70518-0033_47d221be-7385-f815-e063-6294a90a15df
Description

12 TABLET in 1 BLISTER PACK (70518-0033-0)

Marketing

Marketing Status
Marketed Since 2016-12-01
Brand alendronate sodium
Generic alendronate sodium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47d221be-7385-f815-e063-6294a90a15df", "openfda": {"unii": ["2UY4M2U3RA"], "rxcui": ["904431"], "spl_set_id": ["c4358ba7-1bf8-4b0a-9407-5ac279d04555"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BLISTER PACK (70518-0033-0)", "package_ndc": "70518-0033-0", "marketing_start_date": "20161201"}], "brand_name": "ALENDRONATE SODIUM", "product_id": "70518-0033_47d221be-7385-f815-e063-6294a90a15df", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "70518-0033", "generic_name": "Alendronate sodium", "labeler_name": "REMEDYREPACK 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": "20161201", "listing_expiration_date": "20271231"}