NDC 57297-121 Cephalexin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57297 - Lupin Limited
- 57297-121 - Cephalexin
Product Characteristics
GREEN (C48329 - DARK GREEN CAP)
Product Packages
NDC Code 57297-121-01
Package Description: 100 CAPSULE in 1 BOTTLE
NDC Code 57297-121-02
Package Description: 500 CAPSULE in 1 BOTTLE
Product Details
What is NDC 57297-121?
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 ANHYDROUS (UNII: 5SFF1W6677) (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:
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- GELATIN (UNII: 2G86QN327L)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SHELLAC (UNII: 46N107B71O)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
What is the NDC to RxNorm Crosswalk for Cephalexin?
- RxCUI: 309112 - cephalexin 250 MG Oral Capsule
- RxCUI: 309112 - cephalexin (as cephalexin monohydrate) 250 MG Oral Capsule
- RxCUI: 309114 - cephalexin 500 MG Oral Capsule
- RxCUI: 309114 - cefalexin (as cefalexin monohydrate) 500 MG Oral Capsule
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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".