Package 0143-9006-01
Brand: acetazolamide
Generic: acetazolamidePackage Facts
Identity
Package NDC
0143-9006-01
Digits Only
0143900601
Product NDC
0143-9006
Description
1 VIAL in 1 CARTON (0143-9006-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
Marketing
Marketing Status
Brand
acetazolamide
Generic
acetazolamide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "6468455a-a638-4ef0-8bce-41afa7f24c66", "openfda": {"unii": ["429ZT169UH"], "rxcui": ["307702"], "spl_set_id": ["5502e5ba-9b5e-460a-855f-60534b625461"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0143-9006-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "0143-9006-01", "marketing_start_date": "19960501"}], "brand_name": "AcetaZOLAMIDE", "product_id": "0143-9006_6468455a-a638-4ef0-8bce-41afa7f24c66", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "0143-9006", "generic_name": "Acetazolamide", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AcetaZOLAMIDE", "active_ingredients": [{"name": "ACETAZOLAMIDE SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA040089", "marketing_category": "ANDA", "marketing_start_date": "19960501", "listing_expiration_date": "20261231"}