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 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0781-9242
Product ID
0781-9242_2f01d12b-49f3-4310-915d-47710645c96b
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
07819242
Hyphenated Format
0781-9242
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
ANDA061395 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- HOW SUPPLIED Ampicillin for injection, USP for intramuscular or intravenous injection. Ampicillin sodium equivalent to 250 mg, 500 mg, 1 gram, or 2 grams ampicillin per vial. NDC 0781-9242-95 250 mg vial packaged in 10s NDC 0781-9250-95 500 mg vial packaged in 10s NDC 0781-9261-95 1 gram vial packaged in 10s NDC 0781-9273-95 2 gram vial packaged in 10s Storage Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. Protect the constituted solution from freezing. Clinitest is a registered trademark of Miles, Inc. Clinistix is a registered trademark of Bayer Corporation. Tes-Tape is a registered trademark of Eli Lilly Company. PREMIERProRx ® is a registered trademark of Premier Healthcare Alliance, L.P., used under license. Manufactured by Sandoz GmbH for Sandoz Inc., Princeton, NJ 08540 Revised: October 2024
- 250 mg Label NDC 0781- 9242-95 Ampicillin for Injection, USP 250 mg per vial Case Qty.: 10 Vials Rx Only Store the dry powder at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. PREMIER Pro Rx ® 250-mg-case-label
- 500 mg Label NDC 0781- 9250-95 Ampicillin for Injection, USP 500 mg per vial Case Qty.: 10 Vials Rx Only Store the dry powder at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. PREMIER Pro Rx ® 500-mg-case-label
- 1 gram Label NDC 0781- 9261-95 Ampicillin for Injection, USP 1 gram per vial Rx Only For Intramuscular or Intravenous Use 10 x 1 gram Single-Dose Vials PREMIER Pro Rx ® 1-gram-carton-label
- 2 gram Label NDC 0781- 9273-95 Ampicillin for Injection, USP 2 grams per vial Rx Only For Intramuscular or Intravenous Use 10 x 2 grams Single-Dose Vials PREMIER Pro Rx ® 2-grams-carton-label
Packages (0)
No package records.
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "2f01d12b-49f3-4310-915d-47710645c96b", "openfda": {"unii": ["JFN36L5S8K"], "rxcui": ["1721473", "1721474", "1721475", "1721476"], "spl_set_id": ["c2908a44-1da4-4885-ae5a-23f69189d91a"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [], "brand_name": "Ampicillin", "product_id": "0781-9242_2f01d12b-49f3-4310-915d-47710645c96b", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "0781-9242", "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"}