ampicillin
Generic: ampicillin sodium
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
ampicillin
Generic Name
ampicillin sodium
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
ampicillin sodium 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
65219-018
Product ID
65219-018_38c6c088-e4ab-4859-b4d9-89e846cf9d5f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062719
Listing Expiration
2026-12-31
Marketing Start
2020-01-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65219018
Hyphenated Format
65219-018
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
ampicillin (source: ndc)
Generic Name
ampicillin sodium (source: ndc)
Application Number
ANDA062719 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 10 VIAL in 1 CARTON (65219-018-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (65219-018-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "38c6c088-e4ab-4859-b4d9-89e846cf9d5f", "openfda": {"unii": ["JFN36L5S8K"], "rxcui": ["1721473", "1721474", "1721475", "1721476"], "spl_set_id": ["8dbb4c71-8543-08f1-e053-2995a90af88d"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (65219-018-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (65219-018-01)", "package_ndc": "65219-018-10", "marketing_start_date": "20200113"}], "brand_name": "Ampicillin", "product_id": "65219-018_38c6c088-e4ab-4859-b4d9-89e846cf9d5f", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "65219-018", "generic_name": "ampicillin sodium", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ampicillin", "active_ingredients": [{"name": "AMPICILLIN SODIUM", "strength": "1 g/1"}], "application_number": "ANDA062719", "marketing_category": "ANDA", "marketing_start_date": "20200113", "listing_expiration_date": "20261231"}