Package 68788-7130-4

Brand: alendronate sodium

Generic: alendronate sodium
NDC Package

Package Facts

Identity

Package NDC 68788-7130-4
Digits Only 6878871304
Product NDC 68788-7130
Product ID 68788-7130_e88fb31d-cfc6-4e20-95fa-90fa26bf8644
Description

4 TABLET in 1 BLISTER PACK (68788-7130-4)

Marketing

Marketing Status
Marketed Since 2018-03-30
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": "e88fb31d-cfc6-4e20-95fa-90fa26bf8644", "openfda": {"unii": ["2UY4M2U3RA"], "rxcui": ["904431"], "spl_set_id": ["83e3ba94-d882-4b5c-87cb-af1eb0997efc"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BLISTER PACK (68788-7130-4)", "package_ndc": "68788-7130-4", "marketing_start_date": "20180330"}], "brand_name": "ALENDRONATE SODIUM", "product_id": "68788-7130_e88fb31d-cfc6-4e20-95fa-90fa26bf8644", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "68788-7130", "generic_name": "Alendronate sodium", "labeler_name": "Preferred 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": "20180330", "listing_expiration_date": "20271231"}