NDC 50090-4353 Ranitidine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-4353 - Ranitidine
Product Characteristics
Product Packages
NDC Code 50090-4353-0
Package Description: 473 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 50090-4353?
What are the uses for Ranitidine?
Which are Ranitidine UNII Codes?
The UNII codes for the active ingredients in this product are:
- RANITIDINE HYDROCHLORIDE (UNII: BK76465IHM)
- RANITIDINE (UNII: 884KT10YB7) (Active Moiety)
Which are Ranitidine 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:
- ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
- SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM (UNII: GR686LBA74)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM (UNII: 3980JIH2SW)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Ranitidine?
- RxCUI: 705610 - ranitidine 15 MG/ML Oral Solution
- RxCUI: 705610 - ranitidine 15 MG (as ranitidine HCl 16.8 MG) per 1 ML Oral Solution
- RxCUI: 705610 - ranitidine 75 MG per 5 ML Syrup
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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".