Package 67457-446-10

Brand: pamidronate disodium

Generic: pamidronate disodium
NDC Package

Package Facts

Identity

Package NDC 67457-446-10
Digits Only 6745744610
Product NDC 67457-446
Description

1 VIAL in 1 CARTON (67457-446-10) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2011-05-10
Brand pamidronate disodium
Generic pamidronate disodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "e3a78042-50cb-49d9-a31e-51d8edddbf4c", "openfda": {"unii": ["8742T8ZQZA"], "rxcui": ["1737449", "1737453"], "spl_set_id": ["c2ca033e-fa5f-4141-b702-11f8b4303da1"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (67457-446-10)  / 10 mL in 1 VIAL", "package_ndc": "67457-446-10", "marketing_start_date": "20110510"}], "brand_name": "Pamidronate Disodium", "product_id": "67457-446_e3a78042-50cb-49d9-a31e-51d8edddbf4c", "dosage_form": "INJECTION", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "67457-446", "generic_name": "Pamidronate Disodium", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pamidronate Disodium", "active_ingredients": [{"name": "PAMIDRONATE DISODIUM", "strength": "9 mg/mL"}], "application_number": "ANDA078520", "marketing_category": "ANDA", "marketing_start_date": "20110510", "listing_expiration_date": "20271231"}