NDC 54868-3724 Captopril
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-3724 - Captopril
Product Characteristics
WW;172
4
Product Packages
NDC Code 54868-3724-1
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-3724-2
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-3724-3
Package Description: 100 TABLET in 1 BOTTLE
Product Details
What is NDC 54868-3724?
What are the uses for Captopril?
Which are Captopril UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAPTOPRIL (UNII: 9G64RSX1XD)
- CAPTOPRIL (UNII: 9G64RSX1XD) (Active Moiety)
Which are Captopril 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 LACTOSE (UNII: 3SY5LH9PMK)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- STARCH, POTATO (UNII: 8I089SAH3T)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- STARCH, CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Captopril?
- RxCUI: 308962 - captopril 100 MG Oral Tablet
- RxCUI: 308963 - captopril 12.5 MG Oral Tablet
- RxCUI: 308964 - captopril 50 MG Oral Tablet
- RxCUI: 317173 - captopril 25 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".