kit for the preparation of technetium tc99m mertiatide

Generic: betiatide

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name kit for the preparation of technetium tc99m mertiatide
Generic Name betiatide
Labeler sun pharmaceutical industries, inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

betiatide 1 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 45567-0655
Product ID 45567-0655_21ca1be3-2caf-535c-e063-6394a90a18e5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208994
Listing Expiration 2026-12-31
Marketing Start 2019-09-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 455670655
Hyphenated Format 45567-0655

Supplemental Identifiers

UNII
9NV2SR34P8

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name kit for the preparation of technetium tc99m mertiatide (source: ndc)
Generic Name betiatide (source: ndc)
Application Number ANDA208994 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 5 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (45567-0655-1)
source: ndc

Packages (1)

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

Ingredients (1)

betiatide (1 mg/1)

Linked Drug Pages (1)

Kit for the Preparation of Technetium Tc99m Mertiatide ndc-match (0.9)

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"}