Package 0143-9566-01

Brand: azathioprine sodium

Generic: azathioprine sodium
NDC Package

Package Facts

Identity

Package NDC 0143-9566-01
Digits Only 0143956601
Product NDC 0143-9566
Description

1 VIAL in 1 BOX, UNIT-DOSE (0143-9566-01) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 1995-05-01
Brand azathioprine sodium
Generic azathioprine sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0d7e1bc4-3059-47a8-9331-2f37bb3c7b4e", "openfda": {"unii": ["AM94R510MS"], "rxcui": ["239983"], "spl_set_id": ["9ffe79a1-ac91-4a7b-a9e3-7c84bfa9ddf0"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX, UNIT-DOSE (0143-9566-01)  / 10 mL in 1 VIAL", "package_ndc": "0143-9566-01", "marketing_start_date": "19950501"}], "brand_name": "Azathioprine Sodium", "product_id": "0143-9566_0d7e1bc4-3059-47a8-9331-2f37bb3c7b4e", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Nucleic Acid Synthesis Inhibitors [MoA]", "Nucleosides [CS]", "Purine Antimetabolite [EPC]", "Purines [CS]"], "product_ndc": "0143-9566", "generic_name": "Azathioprine Sodium", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azathioprine Sodium", "active_ingredients": [{"name": "AZATHIOPRINE SODIUM", "strength": "100 mg/10mL"}], "application_number": "ANDA074419", "marketing_category": "ANDA", "marketing_start_date": "19950501", "listing_expiration_date": "20261231"}