Package 64980-341-12

Brand: alendronate sodium

Generic: alendronate sodium
NDC Package

Package Facts

Identity

Package NDC 64980-341-12
Digits Only 6498034112
Product NDC 64980-341
Product ID 64980-341_3f943241-8c1a-4261-a337-f2fc45ad2835
Description

3 BLISTER PACK in 1 CARTON (64980-341-12) / 4 TABLET in 1 BLISTER PACK

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": "3f943241-8c1a-4261-a337-f2fc45ad2835", "openfda": {"upc": ["0364980340038", "0364980342148", "0364980342018", "0364980340014"], "unii": ["2UY4M2U3RA"], "rxcui": ["904396", "904419", "904431"], "spl_set_id": ["ffdd2496-d253-419b-85a6-8c615f7545f1"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (64980-341-12)  / 4 TABLET in 1 BLISTER PACK", "package_ndc": "64980-341-12", "marketing_start_date": "20080804"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (64980-341-14)  / 4 TABLET in 1 BLISTER PACK", "package_ndc": "64980-341-14", "marketing_start_date": "20080804"}], "brand_name": "Alendronate Sodium", "product_id": "64980-341_3f943241-8c1a-4261-a337-f2fc45ad2835", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "64980-341", "generic_name": "Alendronate Sodium", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alendronate Sodium", "active_ingredients": [{"name": "ALENDRONATE SODIUM", "strength": "35 mg/1"}], "application_number": "ANDA090124", "marketing_category": "ANDA", "marketing_start_date": "20080804", "listing_expiration_date": "20261231"}