NDC 12634-445 Hydrochlorothiazide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 12634 - Apotheca, Inc.
- 12634-445 - Hydrochlorothiazide
Product Characteristics
Product Packages
NDC Code 12634-445-50
Package Description: 50 TABLET in 1 BOTTLE
NDC Code 12634-445-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 12634-445-71
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 12634-445-78
Package Description: 28 TABLET in 1 BOTTLE
NDC Code 12634-445-79
Package Description: 25 TABLET in 1 BOTTLE
NDC Code 12634-445-85
Package Description: 15 TABLET in 1 BOTTLE
NDC Code 12634-445-90
Package Description: 90 TABLET in 1 BOTTLE
NDC Code 12634-445-91
Package Description: 1 TABLET in 1 BLISTER PACK
Product Details
What is NDC 12634-445?
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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Hydrochlorothiazide?
- RxCUI: 197770 - hydroCHLOROthiazide 50 MG Oral Tablet
- RxCUI: 197770 - hydrochlorothiazide 50 MG Oral Tablet
- RxCUI: 197770 - HCTZ 50 MG Oral Tablet
- RxCUI: 310798 - hydroCHLOROthiazide 25 MG Oral Tablet
- RxCUI: 310798 - hydrochlorothiazide 25 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".