NDC 55648-902 Captopril
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55648 - Wockhardt Limited
- 55648-902 - Captopril
Product Characteristics
Product Packages
NDC Code 55648-902-01
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 55648-902-02
Package Description: 1000 TABLET in 1 BOTTLE
NDC Code 55648-902-05
Package Description: 20000 TABLET in 1 POUCH
Product Details
What is NDC 55648-902?
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)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- PALMITIC ACID (UNII: 2V16EO95H1)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STARCH, CORN (UNII: O8232NY3SJ)
- TALC (UNII: 7SEV7J4R1U)
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".