NDC 67046-651 Ranitidine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 67046-651-07
Package Description: 7 TABLET in 1 BLISTER PACK
NDC Code 67046-651-14
Package Description: 14 TABLET in 1 BLISTER PACK
NDC Code 67046-651-15
Package Description: 15 TABLET in 1 BLISTER PACK
NDC Code 67046-651-20
Package Description: 20 TABLET in 1 BLISTER PACK
NDC Code 67046-651-21
Package Description: 21 TABLET in 1 BLISTER PACK
NDC Code 67046-651-28
Package Description: 28 TABLET in 1 BLISTER PACK
NDC Code 67046-651-30
Package Description: 30 TABLET in 1 BLISTER PACK
NDC Code 67046-651-60
Package Description: 60 TABLET in 1 BLISTER PACK
Product Details
What is NDC 67046-651?
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)
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
- RxCUI: 198193 - ranitidine 300 MG Oral Tablet
- RxCUI: 198193 - ranitidine 300 MG (as ranitidine HCl 336 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".