Ampicillin

Product NDC
0781-9404
11-digit product format
007819404
Labeler code
0781
Product ID
0781-9404_a3ddae6c-ac4c-425f-82b0-eb388d92bc0e
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
Rxcui308207, 1721473, 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
0781-9404-85Ampicillin1 in 1 VIAL, GLASSINJECTION, POWDER, FOR SOLUTION123
0781-9404-95Ampicillin10 in 1 PACKAGEINJECTION, POWDER, FOR SOLUTION1023

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0781-9404-85EA - Each0781-94044362c369-18df-499d-b17f-e75704ade87212012-07-24
0781-9404-95EA - Each0781-9404e6eedebd-e102-470c-90ef-c64ef4daa61c12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AMPICILLIN SODIUMACTIVE INGREDIENTJFN36L5S8KAMPICILLIN (AMPICILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [SANDOZ INC]14
AMPICILLINACTIVE MOIETY7C782967RDAMPICILLIN (AMPICILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [SANDOZ INC]14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0781-9404AMPICILLIN (AMPICILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [SANDOZ INC]23Current NDC, Legacy NDC, 2 package rows20250426_b371e1a5-1fef-4df2-8940-c4fc02b9e2f0.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1721475ampicillin 1 GM InjectionPSNb371e1a5-1fef-4df2-8940-c4fc02b9e2f023
308207ampicillin 125 MG InjectionPSNb371e1a5-1fef-4df2-8940-c4fc02b9e2f023
1721476ampicillin 2 GM InjectionPSNb371e1a5-1fef-4df2-8940-c4fc02b9e2f023
1721473ampicillin 250 MG InjectionPSNb371e1a5-1fef-4df2-8940-c4fc02b9e2f023
1721474ampicillin 500 MG InjectionPSNb371e1a5-1fef-4df2-8940-c4fc02b9e2f023
1721475ampicillin 1000 MG InjectionSCDb371e1a5-1fef-4df2-8940-c4fc02b9e2f023
308207ampicillin 125 MG InjectionSCDb371e1a5-1fef-4df2-8940-c4fc02b9e2f023
1721476ampicillin 2000 MG InjectionSCDb371e1a5-1fef-4df2-8940-c4fc02b9e2f023
1721473ampicillin 250 MG InjectionSCDb371e1a5-1fef-4df2-8940-c4fc02b9e2f023
1721474ampicillin 500 MG InjectionSCDb371e1a5-1fef-4df2-8940-c4fc02b9e2f023
1721475ampicillin (as ampicillin sodium) 1 GM InjectionSYb371e1a5-1fef-4df2-8940-c4fc02b9e2f023
308207ampicillin (as ampicillin sodium) 125 MG InjectionSYb371e1a5-1fef-4df2-8940-c4fc02b9e2f023
1721476ampicillin (as ampicillin sodium) 2 GM InjectionSYb371e1a5-1fef-4df2-8940-c4fc02b9e2f023
1721473ampicillin (as ampicillin sodium) 250 MG InjectionSYb371e1a5-1fef-4df2-8940-c4fc02b9e2f023
1721474ampicillin (as ampicillin sodium) 500 MG InjectionSYb371e1a5-1fef-4df2-8940-c4fc02b9e2f023
1721475ampicillin 1 GM InjectionSYb371e1a5-1fef-4df2-8940-c4fc02b9e2f023
1721476ampicillin 2 GM InjectionSYb371e1a5-1fef-4df2-8940-c4fc02b9e2f023

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0781-9404-85007819404851 in 1 VIAL, GLASSHistorical
0781-9404-950078194049510 VIAL, GLASS in 1 PACKAGE (0781-9404-95) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS (0781-9404-85) 1971-03-030000-00-00NoNoCurrent