NDC 61442-176 Cefaclor
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Product Information
Product Characteristics
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Product Details
What is NDC 61442-176?
What are the uses for Cefaclor?
Which are Cefaclor UNII Codes?
The UNII codes for the active ingredients in this product are:
- CEFACLOR (UNII: 69K7K19H4L)
- CEFACLOR ANHYDROUS (UNII: 3Z6FS3IK0K) (Active Moiety)
Which are Cefaclor 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)
- XANTHAN GUM (UNII: TTV12P4NEE)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Cefaclor?
- RxCUI: 309040 - cefaclor 187 MG in 5 mL Oral Suspension
- RxCUI: 309040 - cefaclor 37.4 MG/ML Oral Suspension
- RxCUI: 309040 - cefaclor 187 MG per 5 ML Oral Suspension
- RxCUI: 309042 - cefaclor 375 MG in 5 mL Oral Suspension
- RxCUI: 309042 - cefaclor 75 MG/ML Oral Suspension
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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".