NDC 55648-986 Cefotaxime
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55648 - Wockhardt Limited
- 55648-986 - Cefotaxime
Product Characteristics
Product Packages
NDC Code 55648-986-02
Package Description: 10 CARTON in 1 CARTON / 1 VIAL, SINGLE-DOSE in 1 CARTON (55648-986-01) / 10 mL in 1 VIAL, SINGLE-DOSE
NDC Code 55648-986-03
Package Description: 25 CARTON in 1 CARTON / 1 VIAL, SINGLE-DOSE in 1 CARTON (55648-986-01) / 10 mL in 1 VIAL, SINGLE-DOSE
NDC Code 55648-986-04
Package Description: 50 CARTON in 1 CARTON / 1 VIAL, SINGLE-DOSE in 1 CARTON (55648-986-01) / 10 mL in 1 VIAL, SINGLE-DOSE
Product Details
What is NDC 55648-986?
What are the uses for Cefotaxime?
Which are Cefotaxime UNII Codes?
The UNII codes for the active ingredients in this product are:
- CEFOTAXIME SODIUM (UNII: 258J72S7TZ)
- CEFOTAXIME (UNII: N2GI8B1GK7) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Cefotaxime?
- RxCUI: 1656313 - cefotaxime 1 GM Injection
- RxCUI: 1656313 - cefotaxime 1000 MG Injection
- RxCUI: 1656313 - cefotaxime (as cefotaxime sodium) 1 GM Injection
- RxCUI: 1656318 - cefotaxime 2 GM Injection
- RxCUI: 1656318 - cefotaxime 2000 MG Injection
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".