ampicillin
Generic: ampicillin
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
ampicillin
Generic Name
ampicillin
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
ampicillin sodium 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1595
Product ID
51662-1595_100d207d-d9fb-7c75-e063-6394a90a53e8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062719
Listing Expiration
2026-12-31
Marketing Start
2022-08-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621595
Hyphenated Format
51662-1595
Supplemental Identifiers
RxCUI
UNII
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 (source: ndc)
Application Number
ANDA062719 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 10 POUCH in 1 CASE (51662-1595-3) / 1 VIAL in 1 POUCH (51662-1595-2) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "100d207d-d9fb-7c75-e063-6394a90a53e8", "openfda": {"unii": ["JFN36L5S8K"], "rxcui": ["1721473"], "spl_set_id": ["e47a21b1-bbdb-4321-e053-2a95a90a3b4a"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "10 POUCH in 1 CASE (51662-1595-3) / 1 VIAL in 1 POUCH (51662-1595-2) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "51662-1595-3", "marketing_start_date": "20220818"}], "brand_name": "AMPICILLIN", "product_id": "51662-1595_100d207d-d9fb-7c75-e063-6394a90a53e8", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "51662-1595", "generic_name": "AMPICILLIN", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMPICILLIN", "active_ingredients": [{"name": "AMPICILLIN SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA062719", "marketing_category": "ANDA", "marketing_start_date": "20220818", "listing_expiration_date": "20261231"}