Package 25021-197-99

Brand: ampicillin sodium

Generic: ampicillin sodium
NDC Package

Package Facts

Identity

Package NDC 25021-197-99
Digits Only 2502119799
Product NDC 25021-197
Description

1 BOTTLE in 1 CARTON (25021-197-99) / 100 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-01-15
Brand ampicillin sodium
Generic ampicillin sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0e1963ba-9650-44ba-9ba0-1817b0e73512", "openfda": {"unii": ["JFN36L5S8K"], "rxcui": ["789980"], "spl_set_id": ["5b3796dd-6f81-4999-ae2b-a13a72795729"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (25021-197-99)  / 100 mL in 1 BOTTLE", "package_ndc": "25021-197-99", "marketing_start_date": "20250115"}], "brand_name": "Ampicillin Sodium", "product_id": "25021-197_0e1963ba-9650-44ba-9ba0-1817b0e73512", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "25021-197", "generic_name": "Ampicillin Sodium", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ampicillin Sodium", "active_ingredients": [{"name": "AMPICILLIN SODIUM", "strength": "10 g/100mL"}], "application_number": "ANDA201404", "marketing_category": "ANDA", "marketing_start_date": "20250115", "listing_expiration_date": "20261231"}