NDC 57297-216 Losartan Potassium And Hydrochlorothiazide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57297 - Lupin Limited
- 57297-216 - Losartan Potassium And Hydrochlorothiazide
Product Characteristics
WHITE (C48325 - WHITE)
OVAL (C48345)
14 MM
LU;M42
Product Packages
NDC Code 57297-216-01
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 57297-216-03
Package Description: 1000 TABLET in 1 BOTTLE
NDC Code 57297-216-06
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 57297-216-09
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 57297-216?
What are the uses for Losartan Potassium And Hydrochlorothiazide?
Which are Losartan Potassium And Hydrochlorothiazide UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH)
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH) (Active Moiety)
- LOSARTAN POTASSIUM (UNII: 3ST302B24A)
- LOSARTAN (UNII: JMS50MPO89) (Active Moiety)
Which are Losartan Potassium 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE (UNII: J2B2A4N98G)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Losartan Potassium And Hydrochlorothiazide?
- RxCUI: 979464 - losartan potassium 100 MG / hydroCHLOROthiazide 12.5 MG Oral Tablet
- RxCUI: 979464 - hydrochlorothiazide 12.5 MG / losartan potassium 100 MG Oral Tablet
- RxCUI: 979464 - HCTZ 12.5 MG / Losartan K+ 100 MG Oral Tablet
- RxCUI: 979464 - HCTZ 12.5 MG / Losartan Pot 100 MG Oral Tablet
- RxCUI: 979464 - HCTZ 12.5 MG / losartan potassium 100 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".