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NDC properties for "Teflaro 400 MG Injection" (RxCUI 1040012)

About this data

The tables show NDC propoerties for Teflaro 400 MG Injection with the RxCUI 1040012

This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product

Details for Teflaro 400 MG Injection (RxCUI 1040012)

MMSL_CODEBD26600
NDANDA200327
RxCUI1040012
SPL_SET_ID3ecde48b-75a2-4beb-9999-369f3f61bb8a
Prescribable SynonymTeflaro 400 MG Injection
RXNAV_STRTeflaro 400 MG Injection
RxNorm Nameceftaroline fosamil 400 MG Injection [Teflaro]
RxNorm SynonymTeflaro 400 MG Injection
Related queriesInteractions (for RxCUI 1040012)



NDC Properties

NDC Item 00456040001

NDC 90456-0400
NDC 100456-0400-01
NDC Item00456040001
Packaging20 mL in 1 VIAL, SINGLE-DOSE
FDA SPL set id811726
LabelerAllergan, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2010-10-29
Marketing statusACTIVE
NDANDA200327
Related queriesProperties for NDC 9 0456-0400

NDC Item 00456040010

NDC 90456-0400
NDC 100456-0400-10
NDC Item00456040010
Packaging10 VIAL, SINGLE-DOSE in 1 CARTON (0456-0400-10) / 20 mL in 1 VIAL, SINGLE-DOSE (0456-0400-01)
FDA SPL set id811726
LabelerAllergan, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2010-10-29
Marketing statusACTIVE
NDANDA200327
Related queriesProperties for NDC 9 0456-0400

NDC Item 00456040001

NDC 90456-0400
NDC 100456-0400-01
NDC Item00456040001
Packaging20 mL in 1 VIAL, SINGLE-DOSE
FDA SPL set id811726
LabelerAllergan, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2010-10-29
Marketing statusACTIVE
NDANDA200327
Related queriesProperties for NDC 9 0456-0400

NDC Item 00456040010

NDC 90456-0400
NDC 100456-0400-10
NDC Item00456040010
Packaging10 VIAL, SINGLE-DOSE in 1 CARTON (0456-0400-10) / 20 mL in 1 VIAL, SINGLE-DOSE (0456-0400-01)
FDA SPL set id811726
LabelerAllergan, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2010-10-29
Marketing statusACTIVE
NDANDA200327
Related queriesProperties for NDC 9 0456-0400