NDC 61442-202 Cephalexin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61442 - Carlsbad Technology, Inc.
- 61442-202 - Cephalexin
Product Characteristics
Product Packages
NDC Code 61442-202-01
Package Description: 24 BOTTLE in 1 BOX / 100 mL in 1 BOTTLE
Price per Unit: $0.13990 per ML
NDC Code 61442-202-02
Package Description: 24 BOTTLE in 1 BOX / 200 mL in 1 BOTTLE
Price per Unit: $0.11232 per ML
Product Details
What is NDC 61442-202?
What are the uses for Cephalexin?
Which are Cephalexin UNII Codes?
The UNII codes for the active ingredients in this product are:
- CEPHALEXIN (UNII: OBN7UDS42Y)
- CEPHALEXIN (UNII: OBN7UDS42Y) (Active Moiety)
Which are Cephalexin Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- METHYLCELLULOSE (25 CPS) (UNII: BI55GG2WLI)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SUCROSE (UNII: C151H8M554)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- STRAWBERRY (UNII: 4J2TY8Y81V)
What is the NDC to RxNorm Crosswalk for Cephalexin?
- RxCUI: 309110 - cephalexin 125 MG in 5 mL Oral Suspension
- RxCUI: 309110 - cephalexin 25 MG/ML Oral Suspension
- RxCUI: 309110 - cefalexin 25 MG/ML Oral Suspension
- RxCUI: 309110 - cephalexin 125 MG per 5 ML Oral Suspension
- RxCUI: 309113 - cephalexin 250 MG in 5 mL Oral Suspension
* Please review the disclaimer below.
[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".