Package 70518-1192-1

Brand: alendronate sodium

Generic: alendronate sodium
NDC Package

Package Facts

Identity

Package NDC 70518-1192-1
Digits Only 7051811921
Product NDC 70518-1192
Product ID 70518-1192_48c078c8-eb3f-84f4-e063-6394a90a8699
Description

3 BLISTER PACK in 1 CARTON (70518-1192-1) / 4 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-01-12
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": "48c078c8-eb3f-84f4-e063-6394a90a8699", "openfda": {"unii": ["2UY4M2U3RA"], "rxcui": ["904396"], "spl_set_id": ["c7e470d6-508e-466e-a78d-060bbbc9745c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (70518-1192-1)  / 4 TABLET in 1 BLISTER PACK", "package_ndc": "70518-1192-1", "marketing_start_date": "20240112"}], "brand_name": "ALENDRONATE SODIUM", "product_id": "70518-1192_48c078c8-eb3f-84f4-e063-6394a90a8699", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "70518-1192", "generic_name": "Alendronate sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALENDRONATE SODIUM", "active_ingredients": [{"name": "ALENDRONATE SODIUM", "strength": "35 mg/1"}], "application_number": "ANDA076768", "marketing_category": "ANDA", "marketing_start_date": "20180516", "listing_expiration_date": "20271231"}