Package 69097-223-76

Brand: alendronate sodium

Generic: alendronate sodium
NDC Package

Package Facts

Identity

Package NDC 69097-223-76
Digits Only 6909722376
Product NDC 69097-223
Product ID 69097-223_1d9a10b4-dc2b-4d58-902a-f202535f4b11
Description

3 BLISTER PACK in 1 CARTON (69097-223-76) / 4 TABLET in 1 BLISTER PACK (69097-223-16)

Marketing

Marketing Status
Marketed Since 2008-08-04
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": "1d9a10b4-dc2b-4d58-902a-f202535f4b11", "openfda": {"unii": ["2UY4M2U3RA"], "rxcui": ["904396", "904431"], "spl_set_id": ["e2fac28d-ad91-4cdc-a003-9fdeac073f76"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (69097-223-76)  / 4 TABLET in 1 BLISTER PACK (69097-223-16)", "package_ndc": "69097-223-76", "marketing_start_date": "20080804"}], "brand_name": "ALENDRONATE SODIUM", "product_id": "69097-223_1d9a10b4-dc2b-4d58-902a-f202535f4b11", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "69097-223", "generic_name": "Alendronate sodium", "labeler_name": "Cipla USA 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": "20080804", "listing_expiration_date": "20271231"}