Package 45567-0655-1

Brand: kit for the preparation of technetium tc99m mertiatide

Generic: betiatide
NDC Package

Package Facts

Identity

Package NDC 45567-0655-1
Digits Only 4556706551
Product NDC 45567-0655
Product ID 45567-0655_21ca1be3-2caf-535c-e063-6394a90a18e5
Description

5 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (45567-0655-1)

Marketing

Marketing Status
Marketed Since 2019-09-02
Brand kit for the preparation of technetium tc99m mertiatide
Generic betiatide
Sample Package No

Linked Drug Pages (1)

Kit for the Preparation of Technetium Tc99m Mertiatide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "21ca1be3-2caf-535c-e063-6394a90a18e5", "openfda": {"unii": ["9NV2SR34P8"], "spl_set_id": ["0ad62039-f848-4f3d-b489-2524e6b6b86e"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (45567-0655-1)", "package_ndc": "45567-0655-1", "marketing_start_date": "20190902"}], "brand_name": "Kit for the Preparation of Technetium Tc99m Mertiatide", "product_id": "45567-0655_21ca1be3-2caf-535c-e063-6394a90a18e5", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "product_ndc": "45567-0655", "generic_name": "Betiatide", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Kit for the Preparation of Technetium Tc99m Mertiatide", "active_ingredients": [{"name": "BETIATIDE", "strength": "1 mg/1"}], "application_number": "ANDA208994", "marketing_category": "ANDA", "marketing_start_date": "20190902", "listing_expiration_date": "20261231"}