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NDC properties for "Teflaro 600 MG Injection" (RxCUI 1040016)

About this data

The tables show NDC propoerties for Teflaro 600 MG Injection with the RxCUI 1040016

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 600 MG Injection (RxCUI 1040016)

MMSL_CODEBD26599
NDANDA200327
RxCUI1040016
SPL_SET_ID3ecde48b-75a2-4beb-9999-369f3f61bb8a
Prescribable SynonymTeflaro 600 MG Injection
RXNAV_STRTeflaro 600 MG Injection
RxNorm Nameceftaroline fosamil 600 MG Injection [Teflaro]
RxNorm SynonymTeflaro 600 MG Injection
Related queriesInteractions (for RxCUI 1040016)



NDC Properties

NDC Item 00456060001

NDC 90456-0600
NDC 100456-0600-01
NDC Item00456060001
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 0456-0600

NDC Item 00456060010

NDC 90456-0600
NDC 100456-0600-10
NDC Item00456060010
Packaging10 VIAL, SINGLE-DOSE in 1 CARTON (0456-0600-10) / 20 mL in 1 VIAL, SINGLE-DOSE (0456-0600-01)
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 0456-0600

NDC Item 00456060001

NDC 90456-0600
NDC 100456-0600-01
NDC Item00456060001
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 0456-0600

NDC Item 00456060010

NDC 90456-0600
NDC 100456-0600-10
NDC Item00456060010
Packaging10 VIAL, SINGLE-DOSE in 1 CARTON (0456-0600-10) / 20 mL in 1 VIAL, SINGLE-DOSE (0456-0600-01)
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 0456-0600