ampicillin
Generic: ampicillin
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
ampicillin
Generic Name
ampicillin
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
ampicillin sodium 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
25021-136
Product ID
25021-136_c3bd533d-1831-4030-8fc0-97c93f4803b6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090354
Listing Expiration
2026-12-31
Marketing Start
2014-07-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021136
Hyphenated Format
25021-136
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 (source: ndc)
Application Number
ANDA090354 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 10 VIAL in 1 CARTON (25021-136-10) / 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": "c3bd533d-1831-4030-8fc0-97c93f4803b6", "openfda": {"unii": ["JFN36L5S8K"], "rxcui": ["1721475", "1721476"], "spl_set_id": ["9d2aebe8-4f04-49dd-b1e5-80b962868dc3"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-136-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "25021-136-10", "marketing_start_date": "20140701"}], "brand_name": "ampicillin", "product_id": "25021-136_c3bd533d-1831-4030-8fc0-97c93f4803b6", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "25021-136", "generic_name": "ampicillin", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ampicillin", "active_ingredients": [{"name": "AMPICILLIN SODIUM", "strength": "1 g/1"}], "application_number": "ANDA090354", "marketing_category": "ANDA", "marketing_start_date": "20140701", "listing_expiration_date": "20261231"}