ampicillin

Generic: ampicillin injection

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ampicillin
Generic Name ampicillin injection
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

ampicillin sodium 250 mg/250mg

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-914
Product ID 23155-914_65071c52-ece6-4774-a50f-ce981776b5e6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090354
Listing Expiration 2026-12-31
Marketing Start 2025-01-31

Pharmacologic Class

Classes
penicillin-class antibacterial [epc] penicillins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155914
Hyphenated Format 23155-914

Supplemental Identifiers

RxCUI
1721473 1721474 1721475 1721476
UNII
JFN36L5S8K

Packaging Origin

Original Packager
true

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 injection (source: ndc)
Application Number ANDA090354 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 250 mg/250mg
source: ndc
Packaging
  • 10 VIAL in 1 PACKAGE (23155-914-41) / 250 mg in 1 VIAL (23155-914-31)
source: ndc

Packages (1)

Ingredients (1)

ampicillin sodium (250 mg/250mg)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "65071c52-ece6-4774-a50f-ce981776b5e6", "openfda": {"unii": ["JFN36L5S8K"], "rxcui": ["1721473", "1721474", "1721475", "1721476"], "spl_set_id": ["302e6df7-37c5-4625-8a61-3e2f302addf2"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 PACKAGE (23155-914-41)  / 250 mg in 1 VIAL (23155-914-31)", "package_ndc": "23155-914-41", "marketing_start_date": "20250131"}], "brand_name": "AMPICILLIN", "product_id": "23155-914_65071c52-ece6-4774-a50f-ce981776b5e6", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "23155-914", "generic_name": "Ampicillin Injection", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMPICILLIN", "active_ingredients": [{"name": "AMPICILLIN SODIUM", "strength": "250 mg/250mg"}], "application_number": "ANDA090354", "marketing_category": "ANDA", "marketing_start_date": "20250131", "listing_expiration_date": "20261231"}