Package 0781-9412-92
Brand: ampicillin
Generic: ampicillin sodiumPackage Facts
Identity
Package NDC
0781-9412-92
Digits Only
0781941292
Product NDC
0781-9412
Description
10 VIAL, GLASS in 1 PACKAGE (0781-9412-92) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0781-9412-15)
Marketing
Marketing Status
Brand
ampicillin
Generic
ampicillin sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f1afd007-8e8c-40e2-b353-8def35a0ce8b", "openfda": {"unii": ["JFN36L5S8K"], "rxcui": ["1721475", "1721476"], "spl_set_id": ["f77db491-31c4-4a7c-a114-0f3244c97090"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, GLASS in 1 PACKAGE (0781-9412-92) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0781-9412-15)", "package_ndc": "0781-9412-92", "marketing_start_date": "19870219"}], "brand_name": "Ampicillin", "product_id": "0781-9412_f1afd007-8e8c-40e2-b353-8def35a0ce8b", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "0781-9412", "generic_name": "Ampicillin Sodium", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ampicillin", "active_ingredients": [{"name": "AMPICILLIN SODIUM", "strength": "1 g/1"}], "application_number": "ANDA062738", "marketing_category": "ANDA", "marketing_start_date": "19870219", "listing_expiration_date": "20261231"}