NDC 54868-3906 Benazepril Hydrochloride And Hydrochlorothiazide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-3906 - Benazepril Hydrochloride And Hydrochlorothiazide
Product Characteristics
PURPLE (C48327 - (LAVENDER))
E211
Product Packages
NDC Code 54868-3906-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
NDC Code 54868-3906-1
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
NDC Code 54868-3906-2
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-3906?
What are the uses for Benazepril Hydrochloride And Hydrochlorothiazide?
Which are Benazepril Hydrochloride And Hydrochlorothiazide UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENAZEPRIL HYDROCHLORIDE (UNII: N1SN99T69T)
- BENAZEPRILAT (UNII: JRM708L703) (Active Moiety)
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH)
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH) (Active Moiety)
Which are Benazepril Hydrochloride 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:
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSPOVIDONE (UNII: 68401960MK)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- POLOXAMER 188 (UNII: LQA7B6G8JG)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ZINC STEARATE (UNII: H92E6QA4FV)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Benazepril Hydrochloride And Hydrochlorothiazide?
- RxCUI: 898362 - benazepril HCl 10 MG / hydroCHLOROthiazide 12.5 MG Oral Tablet
- RxCUI: 898362 - benazepril hydrochloride 10 MG / hydrochlorothiazide 12.5 MG Oral Tablet
- RxCUI: 898362 - benazepril hydrochloride 10 MG / HCTZ 12.5 MG Oral Tablet
- RxCUI: 898362 - BZP hydrochloride 10 MG / HCTZ 12.5 MG Oral Tablet
- RxCUI: 898367 - benazepril HCl 20 MG / hydroCHLOROthiazide 12.5 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".