ampicillin

Generic: ampicillin

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ampicillin
Generic Name ampicillin
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

ampicillin sodium 250 mg/1

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

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
penicillin-class antibacterial [epc] penicillins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621595
Hyphenated Format 51662-1595

Supplemental Identifiers

RxCUI
1721473
UNII
JFN36L5S8K

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
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
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
source: ndc

Packages (1)

Ingredients (1)

ampicillin sodium (250 mg/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"}