NDC 50436-6930 Ranitidine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 50436-6930?
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:
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
What is the NDC to RxNorm Crosswalk for Ranitidine?
- RxCUI: 198191 - ranitidine 150 MG Oral Tablet
- RxCUI: 198191 - ranitidine 150 MG (as ranitidine HCl 168 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".