NDC 33261-109 Lisinopril
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33261 - Aidarex Pharmaceuticals Llc
- 33261-109 - Lisinopril
Product Characteristics
RED (C48326)
YELLOW (C48330)
9 MM
LUPIN;30
LUPIN;40
Product Packages
NDC Code 33261-109-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 33261-109-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 33261-109?
What are the uses for Lisinopril?
Which are Lisinopril UNII Codes?
The UNII codes for the active ingredients in this product are:
- LISINOPRIL (UNII: E7199S1YWR)
- LISINOPRIL ANHYDROUS (UNII: 7Q3P4BS2FD) (Active Moiety)
Which are Lisinopril 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:
- CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)
- MANNITOL (UNII: 3OWL53L36A)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STARCH, CORN (UNII: O8232NY3SJ)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Lisinopril?
- RxCUI: 197884 - lisinopril 40 MG Oral Tablet
- RxCUI: 205326 - lisinopril 30 MG Oral Tablet
- RxCUI: 314076 - lisinopril 10 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".