NDC 64725-0045 Hydrochlorothiazide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64725 - Tya Pharmaceuticals
- 64725-0045 - Hydrochlorothiazide
Product Characteristics
Product Packages
NDC Code 64725-0045-1
Package Description: 100 CAPSULE in 1 BOTTLE
Product Details
What is NDC 64725-0045?
What are the uses for Hydrochlorothiazide?
Which are Hydrochlorothiazide UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH)
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH) (Active Moiety)
Which are 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:
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- GELATIN (UNII: 2G86QN327L)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- STARCH, CORN (UNII: O8232NY3SJ)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
What is the NDC to RxNorm Crosswalk for Hydrochlorothiazide?
- RxCUI: 199903 - hydroCHLOROthiazide 12.5 MG Oral Capsule
- RxCUI: 199903 - hydrochlorothiazide 12.5 MG Oral Capsule
- RxCUI: 199903 - HCTZ 12.5 MG Oral Capsule
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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".