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NDC properties for "ceftaroline fosamil 400 MG Injection" (RxCUI 1040008)

About this data

The tables show NDC propoerties for ceftaroline fosamil 400 MG Injection with the RxCUI 1040008

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 400 MG Injection (RxCUI 1040008)

ANDAANDA208075
MMSL_CODECD26600
RxCUI1040008
SPL_SET_ID3cee3c08-ed60-06c5-ac49-103b7ad2ef5f
VUID4030285
Prescribable Synonymceftaroline fosamil 400 MG Injection
RXNAV_STRceftaroline fosamil 400 MG Injection
RxNorm Nameceftaroline fosamil 400 MG Injection
Related queriesInteractions (for RxCUI 1040008)



NDC Properties

NDC Item 60505612400

NDC 960505-6124
NDC 1060505-6124-0
NDC Item60505612400
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 60505-6124

NDC Item 60505612401

NDC 960505-6124
NDC 1060505-6124-1
NDC Item60505612401
Packaging10 VIAL, SINGLE-DOSE in 1 CARTON (60505-6124-1) / 20 mL in 1 VIAL, SINGLE-DOSE (60505-6124-0)
ANDAANDA208075
LabelerApotex Corp.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2026-02-12
Marketing statusACTIVE
Related queriesProperties for NDC 9 60505-6124

NDC Item 60505612400

NDC 960505-6124
NDC 1060505-6124-0
NDC Item60505612400
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 60505-6124

NDC Item 60505612401

NDC 960505-6124
NDC 1060505-6124-1
NDC Item60505612401
Packaging10 VIAL, SINGLE-DOSE in 1 CARTON (60505-6124-1) / 20 mL in 1 VIAL, SINGLE-DOSE (60505-6124-0)
ANDAANDA208075
LabelerApotex Corp.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2026-02-12
Marketing statusACTIVE
Related queriesProperties for NDC 9 60505-6124