Ampicillin

Product NDC
0781-9261
11-digit product format
007819261
Labeler code
0781
Product ID
0781-9261_2f01d12b-49f3-4310-915d-47710645c96b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ampicillin sodium
Dosage form
INJECTION, POWDER, FOR SOLUTION
Route
INTRAMUSCULAR; INTRAVENOUS
Labeler
Sandoz Inc
Application
ANDA061395
Marketing category
ANDA
Marketing start
1971-03-03
Substance
AMPICILLIN SODIUM
Active strength
1 g/1
Pharmacologic classes
Penicillin-class Antibacterial [EPC], Penicillins [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Ampicillin
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AMPICILLIN SODIUM1 g/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiJFN36L5S8K
Rxcui1721473, 1721474, 1721475, 1721476

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fd9d6ee0-43ae-43c7-aa52-3d5a936186d6Product name120250722
4fe9b92f-7dcd-4058-8def-e75f4dcd5ab3Product name220160201
c9385d77-2af7-47a4-bc97-1127e71caf9bProduct name320160201
05b6b9ae-4ba4-27ee-4c8c-f72b41de3815Product name520151207
b353113e-7b3d-4b1f-a286-b96a3a5eac85Product name320151026
8c59be9b-72b0-49e8-b7ef-1a80c10599deProduct name320150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0781-9261-85Ampicillin1 in 1 VIAL, GLASSINJECTION, POWDER, FOR SOLUTION118
0781-9261-95Ampicillin10 in 1 PACKAGEINJECTION, POWDER, FOR SOLUTION1018

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0781-9261-85EA - Each0781-926114d17983-f581-43b6-841e-f65d94fd180b12016-01-13
0781-9261-95EA - Each0781-92614a2b4e79-75d5-4ff5-ac2f-d6365301061712016-01-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AMPICILLIN SODIUMACTIVE INGREDIENTJFN36L5S8KAMPICILLIN (AMPICILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [SANDOZ INC]10
AMPICILLINACTIVE MOIETY7C782967RDAMPICILLIN (AMPICILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [SANDOZ INC]10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0781-9261AMPICILLIN (AMPICILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [SANDOZ INC]18Current NDC, Legacy NDC, 2 package rows20250426_c2908a44-1da4-4885-ae5a-23f69189d91a.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1721475ampicillin 1 GM InjectionPSNc2908a44-1da4-4885-ae5a-23f69189d91a18
1721476ampicillin 2 GM InjectionPSNc2908a44-1da4-4885-ae5a-23f69189d91a18
1721473ampicillin 250 MG InjectionPSNc2908a44-1da4-4885-ae5a-23f69189d91a18
1721474ampicillin 500 MG InjectionPSNc2908a44-1da4-4885-ae5a-23f69189d91a18
1721475ampicillin 1000 MG InjectionSCDc2908a44-1da4-4885-ae5a-23f69189d91a18
1721476ampicillin 2000 MG InjectionSCDc2908a44-1da4-4885-ae5a-23f69189d91a18
1721473ampicillin 250 MG InjectionSCDc2908a44-1da4-4885-ae5a-23f69189d91a18
1721474ampicillin 500 MG InjectionSCDc2908a44-1da4-4885-ae5a-23f69189d91a18
1721475ampicillin (as ampicillin sodium) 1 GM InjectionSYc2908a44-1da4-4885-ae5a-23f69189d91a18
1721476ampicillin (as ampicillin sodium) 2 GM InjectionSYc2908a44-1da4-4885-ae5a-23f69189d91a18
1721473ampicillin (as ampicillin sodium) 250 MG InjectionSYc2908a44-1da4-4885-ae5a-23f69189d91a18
1721474ampicillin (as ampicillin sodium) 500 MG InjectionSYc2908a44-1da4-4885-ae5a-23f69189d91a18
1721475ampicillin 1 GM InjectionSYc2908a44-1da4-4885-ae5a-23f69189d91a18
1721476ampicillin 2 GM InjectionSYc2908a44-1da4-4885-ae5a-23f69189d91a18

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0781-9261-85007819261851 in 1 VIAL, GLASSHistorical
0781-9261-950078192619510 VIAL, GLASS in 1 PACKAGE (0781-9261-95) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0781-9261-85) 2015-04-280000-00-00NoNoCurrent