ampicillin
Generic: ampicillin injection
Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.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
Active Ingredients
ampicillin sodium 250 mg/250mg
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
23155914
Hyphenated Format
23155-914
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 injection (source: ndc)
Application Number
ANDA090354 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/250mg
Packaging
- 10 VIAL in 1 PACKAGE (23155-914-41) / 250 mg in 1 VIAL (23155-914-31)
Packages (1)
Ingredients (1)
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"}