NDC 57297-402 Cefprozil
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57297 - Lupin Limited
- 57297-402 - Cefprozil
Product Characteristics
Product Packages
NDC Code 57297-402-01
Package Description: 50 mL in 1 BOTTLE
NDC Code 57297-402-02
Package Description: 75 mL in 1 BOTTLE
NDC Code 57297-402-03
Package Description: 100 mL in 1 BOTTLE
Product Details
What is NDC 57297-402?
What are the uses for Cefprozil?
Which are Cefprozil UNII Codes?
The UNII codes for the active ingredients in this product are:
- CEFPROZIL (UNII: 4W0459ZA4V)
- CEFPROZIL ANHYDROUS (UNII: 1M698F4H4E) (Active Moiety)
Which are Cefprozil 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- ASPARTAME (UNII: Z0H242BBR1)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GLYCINE (UNII: TE7660XO1C)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SUCROSE (UNII: C151H8M554)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
What is the NDC to RxNorm Crosswalk for Cefprozil?
- RxCUI: 309080 - cefprozil 125 MG in 5 mL Oral Suspension
- RxCUI: 309080 - cefprozil 25 MG/ML Oral Suspension
- RxCUI: 309080 - cefprozil 125 MG per 5 ML Oral Suspension
- RxCUI: 309081 - cefprozil 250 MG in 5 mL Oral Suspension
- RxCUI: 309081 - cefprozil 50 MG/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".