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NDC properties for "ceftaroline fosamil 600 MG Injection" (RxCUI 1040014)

About this data

The tables show NDC propoerties for ceftaroline fosamil 600 MG Injection with the RxCUI 1040014

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 ceftaroline fosamil 600 MG Injection (RxCUI 1040014)

ANDAANDA208075
MMSL_CODECD26599
RxCUI1040014
SNOMEDCT1236785003
SPL_SET_ID3cee3c08-ed60-06c5-ac49-103b7ad2ef5f
VUID4030286
Prescribable Synonymceftaroline fosamil 600 MG Injection
RXNAV_STRceftaroline fosamil 600 MG Injection
RxNorm Nameceftaroline fosamil 600 MG Injection
Related queriesInteractions (for RxCUI 1040014)



NDC Properties

NDC Item 60505612500

NDC 960505-6125
NDC 1060505-6125-0
NDC Item60505612500
Packaging20 mL in 1 VIAL, SINGLE-DOSE
ANDAANDA208075
LabelerApotex Corp.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2026-02-12
Marketing statusACTIVE
Related queriesProperties for NDC 9 60505-6125

NDC Item 60505612501

NDC 960505-6125
NDC 1060505-6125-1
NDC Item60505612501
Packaging10 VIAL, SINGLE-DOSE in 1 CARTON (60505-6125-1) / 20 mL in 1 VIAL, SINGLE-DOSE (60505-6125-0)
ANDAANDA208075
LabelerApotex Corp.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2026-02-12
Marketing statusACTIVE
Related queriesProperties for NDC 9 60505-6125

NDC Item 60505612500

NDC 960505-6125
NDC 1060505-6125-0
NDC Item60505612500
Packaging20 mL in 1 VIAL, SINGLE-DOSE
ANDAANDA208075
LabelerApotex Corp.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2026-02-12
Marketing statusACTIVE
Related queriesProperties for NDC 9 60505-6125

NDC Item 60505612501

NDC 960505-6125
NDC 1060505-6125-1
NDC Item60505612501
Packaging10 VIAL, SINGLE-DOSE in 1 CARTON (60505-6125-1) / 20 mL in 1 VIAL, SINGLE-DOSE (60505-6125-0)
ANDAANDA208075
LabelerApotex Corp.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2026-02-12
Marketing statusACTIVE
Related queriesProperties for NDC 9 60505-6125