Package 70436-019-82

Brand: azithromycin

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 70436-019-82
Digits Only 7043601982
Product NDC 70436-019
Description

10 VIAL in 1 BOX (70436-019-82) / 5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2018-12-19
Brand azithromycin
Generic azithromycin dihydrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ebe5ec1e-9891-ae48-e053-2a95a90afff6", "openfda": {"upc": ["0370436019823"], "unii": ["5FD1131I7S"], "rxcui": ["1668238"], "spl_set_id": ["8acce3c1-f4be-4968-a71f-3ffd9fbaa4a4"], "manufacturer_name": ["Slate Run Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 BOX (70436-019-82)  / 5 mL in 1 VIAL", "package_ndc": "70436-019-82", "marketing_start_date": "20181219"}], "brand_name": "Azithromycin", "product_id": "70436-019_ebe5ec1e-9891-ae48-e053-2a95a90afff6", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "70436-019", "generic_name": "Azithromycin Dihydrate", "labeler_name": "Slate Run Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/5mL"}], "application_number": "ANDA203412", "marketing_category": "ANDA", "marketing_start_date": "20181219", "listing_expiration_date": "20261231"}