NDC 55648-712 Cefprozil
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55648 - Wockhardt Limited
- 55648-712 - Cefprozil
Product Characteristics
Product Packages
NDC Code 55648-712-01
Package Description: 50 TABLET, FILM COATED in 1 BOTTLE
NDC Code 55648-712-02
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE
NDC Code 55648-712-03
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE
NDC Code 55648-712-04
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 55648-712?
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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED (UNII: 2165RE0K14)
- HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHYLCELLULOSE (15 CPS) (UNII: NPU9M2E6L8)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Cefprozil?
- RxCUI: 197452 - cefprozil 250 MG Oral Tablet
- RxCUI: 197453 - cefprozil 500 MG Oral Tablet
* 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".