Package 82449-515-01

Brand: ampicillin

Generic: ampicillin
NDC Package

Package Facts

Identity

Package NDC 82449-515-01
Digits Only 8244951501
Product NDC 82449-515
Description

1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (82449-515-01)

Marketing

Marketing Status
Marketed Since 2025-05-01
Brand ampicillin
Generic ampicillin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "35b4dd5c-331d-f591-e063-6394a90ae874", "openfda": {"unii": ["JFN36L5S8K"], "rxcui": ["789980"], "spl_set_id": ["f23b2408-a04e-4a8d-93ca-4d1c9a807e18"], "manufacturer_name": ["Steriscience Specialties Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (82449-515-01)", "package_ndc": "82449-515-01", "marketing_start_date": "20250501"}], "brand_name": "Ampicillin", "product_id": "82449-515_35b4dd5c-331d-f591-e063-6394a90ae874", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "82449-515", "generic_name": "Ampicillin", "labeler_name": "Steriscience Specialties Private Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ampicillin", "active_ingredients": [{"name": "AMPICILLIN SODIUM", "strength": "10 g/1"}], "application_number": "ANDA202198", "marketing_category": "ANDA", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}