ampicillin

Generic: ampicillin sodium

Labeler: sandoz inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ampicillin
Generic Name ampicillin sodium
Labeler sandoz inc
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

ampicillin sodium 250 mg/1

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 0781-3402
Product ID 0781-3402_2cc1b620-59dd-4d45-8edf-af20bdd82ee5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA061395
Listing Expiration 2026-12-31
Marketing Start 1971-03-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 07813402
Hyphenated Format 0781-3402

Supplemental Identifiers

RxCUI
308207 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 sodium (source: ndc)
Application Number ANDA061395 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 10 VIAL, GLASS in 1 PACKAGE (0781-3402-95) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0781-3402-78)
source: ndc

Packages (1)

0781-3402-95 10 VIAL, GLASS in 1 PACKAGE (0781-3402-95) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0781-3402-78)

Ingredients (1)

ampicillin sodium (250 mg/1)

Linked Drug Pages (1)

Ampicillin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "2cc1b620-59dd-4d45-8edf-af20bdd82ee5", "openfda": {"unii": ["JFN36L5S8K"], "rxcui": ["308207", "1721473", "1721474", "1721475", "1721476"], "spl_set_id": ["64a04e8c-8f78-46b3-8f45-56ef225a4f74"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, GLASS in 1 PACKAGE (0781-3402-95)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0781-3402-78)", "package_ndc": "0781-3402-95", "marketing_start_date": "19710303"}], "brand_name": "Ampicillin", "product_id": "0781-3402_2cc1b620-59dd-4d45-8edf-af20bdd82ee5", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "0781-3402", "generic_name": "Ampicillin sodium", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ampicillin", "active_ingredients": [{"name": "AMPICILLIN SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA061395", "marketing_category": "ANDA", "marketing_start_date": "19710303", "listing_expiration_date": "20261231"}