NDC 54868-4977 Lisinopril And Hydrochlorothiazide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
BLUE (C48333)
6 MM
RX536
Code Structure Chart
Product Details
What is NDC 54868-4977?
What are the uses for Lisinopril And Hydrochlorothiazide?
Which are Lisinopril And Hydrochlorothiazide UNII Codes?
The UNII codes for the active ingredients in this product are:
- LISINOPRIL (UNII: E7199S1YWR)
- LISINOPRIL (UNII: E7199S1YWR) (Active Moiety)
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH)
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH) (Active Moiety)
Which are Lisinopril And Hydrochlorothiazide 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:
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
- STARCH, CORN (UNII: O8232NY3SJ)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
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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".