Aztreonam

Product NDC
0409-0829
11-digit product format
004090829
Labeler code
0409
Product ID
0409-0829_8664bd65-dcd7-420f-a8e3-01eaf3e02b36
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Aztreonam
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAMUSCULAR; INTRAVENOUS
Labeler
Hospira, Inc.
Application
ANDA206517
Marketing category
ANDA
Marketing start
2022-01-24
Substance
AZTREONAM
Active strength
1 g/1
Pharmacologic classes
Monobactam Antibacterial [EPC], Monobactams [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AZTREONAM1 g/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG2B4VE5GH8
Rxcui1664981, 1664986

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
458b18b0-b105-44ac-b090-378873a4e07bProduct name120251118
882349af-ee4e-3057-6dd7-68d0b142db19Product name220220608
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508
74c5690d-3e83-e116-f1e7-47b67331bf80Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0409-0829-01Aztreonam10 in 1 CARTONINJECTION, POWDER, LYOPHILIZED,103
0409-0829-11Aztreonam1 in 1 VIAL, SINGLE-DOSEINJECTION, POWDER, LYOPHILIZED,13

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0409-0829-01EA - Each0409-0829f421bf9d-2130-4dec-935d-5c5ed1a69dd512022-02-07
0409-0829-11EA - Each0409-082967a465cb-2195-43e4-acad-cc0b2b51b48412022-02-07

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0409-0829AZTREONAM INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [HOSPIRA, INC.]3Current NDC, Legacy NDC, 2 package rows20240616_d4500795-3b07-4a7d-b432-73cafbb3dbc6.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1664981aztreonam 1 GM InjectionPSNd4500795-3b07-4a7d-b432-73cafbb3dbc63
1664986aztreonam 2 GM InjectionPSNd4500795-3b07-4a7d-b432-73cafbb3dbc63
1664981aztreonam 1000 MG InjectionSCDd4500795-3b07-4a7d-b432-73cafbb3dbc63
1664986aztreonam 2000 MG InjectionSCDd4500795-3b07-4a7d-b432-73cafbb3dbc63

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0409-0829-010040908290110 VIAL, SINGLE-DOSE in 1 CARTON (0409-0829-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (0409-0829-11) 2022-01-240000-00-00NoNoCurrent
0409-0829-11004090829111 in 1 VIAL, SINGLE-DOSEHistorical