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 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
0781-9412
Product ID
0781-9412_f1afd007-8e8c-40e2-b353-8def35a0ce8b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062738
Listing Expiration
2026-12-31
Marketing Start
1987-02-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07819412
Hyphenated Format
0781-9412
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 sodium (source: ndc)
Application Number
ANDA062738 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 10 VIAL, GLASS in 1 PACKAGE (0781-9412-92) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0781-9412-15)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f1afd007-8e8c-40e2-b353-8def35a0ce8b", "openfda": {"unii": ["JFN36L5S8K"], "rxcui": ["1721475", "1721476"], "spl_set_id": ["f77db491-31c4-4a7c-a114-0f3244c97090"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, GLASS in 1 PACKAGE (0781-9412-92) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0781-9412-15)", "package_ndc": "0781-9412-92", "marketing_start_date": "19870219"}], "brand_name": "Ampicillin", "product_id": "0781-9412_f1afd007-8e8c-40e2-b353-8def35a0ce8b", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "0781-9412", "generic_name": "Ampicillin Sodium", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ampicillin", "active_ingredients": [{"name": "AMPICILLIN SODIUM", "strength": "1 g/1"}], "application_number": "ANDA062738", "marketing_category": "ANDA", "marketing_start_date": "19870219", "listing_expiration_date": "20261231"}