NDC 21695-638 Phenazopyridine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-638 - Phenazopyridine Hydrochloride
Product Characteristics
Product Packages
NDC Code 21695-638-10
Package Description: 10 TABLET in 1 BOTTLE
NDC Code 21695-638-15
Package Description: 15 TABLET in 1 BOTTLE
NDC Code 21695-638-30
Package Description: 30 TABLET in 1 BOTTLE
Product Details
What is NDC 21695-638?
What are the uses for Phenazopyridine Hydrochloride?
Which are Phenazopyridine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHENAZOPYRIDINE HYDROCHLORIDE (UNII: 0EWG668W17)
- PHENAZOPYRIDINE (UNII: K2J09EMJ52) (Active Moiety)
Which are Phenazopyridine 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:
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- STARCH, CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Phenazopyridine Hydrochloride?
- RxCUI: 1094104 - phenazopyridine HCl 200 MG Oral Tablet
- RxCUI: 1094104 - phenazopyridine hydrochloride 200 MG Oral Tablet
- RxCUI: 1094107 - phenazopyridine HCl 100 MG Oral Tablet
- RxCUI: 1094107 - phenazopyridine hydrochloride 100 MG Oral Tablet
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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".