ampicillin
Generic: ampicillin sodium
Labeler: sandoz incDrug Facts
Product Profile
Brand Name
ampicillin
Generic Name
ampicillin sodium
Labeler
sandoz inc
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
ampicillin sodium 10 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
0781-9409
Product ID
0781-9409_86e9a3cc-bc65-4d4f-916d-98c916588730
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA061395
Listing Expiration
2026-12-31
Marketing Start
1971-03-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07819409
Hyphenated Format
0781-9409
Supplemental Identifiers
RxCUI
UPC
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 sodium (source: ndc)
Application Number
ANDA061395 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 g/1
Packaging
- 10 VIAL, PHARMACY BULK PACKAGE in 1 PACKAGE (0781-9409-95) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PHARMACY BULK PACKAGE (0781-9409-46)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "86e9a3cc-bc65-4d4f-916d-98c916588730", "openfda": {"upc": ["0307819409957"], "unii": ["JFN36L5S8K"], "rxcui": ["789980"], "spl_set_id": ["5308ddfa-4a5b-4f7b-83ce-9d1b528e050d"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, PHARMACY BULK PACKAGE in 1 PACKAGE (0781-9409-95) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PHARMACY BULK PACKAGE (0781-9409-46)", "package_ndc": "0781-9409-95", "marketing_start_date": "19710303"}], "brand_name": "Ampicillin", "product_id": "0781-9409_86e9a3cc-bc65-4d4f-916d-98c916588730", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "0781-9409", "generic_name": "Ampicillin Sodium", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ampicillin", "active_ingredients": [{"name": "AMPICILLIN SODIUM", "strength": "10 g/1"}], "application_number": "ANDA061395", "marketing_category": "ANDA", "marketing_start_date": "19710303", "listing_expiration_date": "20261231"}