NDC 67046-209 Prazosin Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67046 - Contract Pharmacy Services-pa
- 67046-209 - Prazosin Hydrochloride
Product Characteristics
BROWN (C48332 - LIGHT BROWN OPAQUE)
Product Packages
NDC Code 67046-209-07
Package Description: 7 CAPSULE in 1 BLISTER PACK
NDC Code 67046-209-14
Package Description: 14 CAPSULE in 1 BLISTER PACK
NDC Code 67046-209-15
Package Description: 15 CAPSULE in 1 BLISTER PACK
NDC Code 67046-209-20
Package Description: 20 CAPSULE in 1 BLISTER PACK
NDC Code 67046-209-21
Package Description: 21 CAPSULE in 1 BLISTER PACK
NDC Code 67046-209-28
Package Description: 28 CAPSULE in 1 BLISTER PACK
NDC Code 67046-209-30
Package Description: 30 CAPSULE in 1 BLISTER PACK
NDC Code 67046-209-60
Package Description: 60 CAPSULE in 1 BLISTER PACK
Product Details
What is NDC 67046-209?
What are the uses for Prazosin Hydrochloride?
Which are Prazosin Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- PRAZOSIN HYDROCHLORIDE (UNII: X0Z7454B90)
- PRAZOSIN (UNII: XM03YJ541D) (Active Moiety)
Which are Prazosin Hydrochloride 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- GELATIN (UNII: 2G86QN327L)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- AMMONIA (UNII: 5138Q19F1X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- DIMETHICONE (UNII: 92RU3N3Y1O)
What is the NDC to RxNorm Crosswalk for Prazosin Hydrochloride?
- RxCUI: 312593 - prazosin HCl 1 MG Oral Capsule
- RxCUI: 312593 - prazosin 1 MG Oral Capsule
- RxCUI: 312593 - prazosin (as prazosin HCl) 1 MG Oral Capsule
- RxCUI: 312594 - prazosin HCl 2 MG Oral Capsule
- RxCUI: 312594 - prazosin 2 MG Oral Capsule
* 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".