NDC 33261-202 Ranitidine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33261 - Aidarex Pharmaceuticals Llc
- 33261-202 - Ranitidine
Product Characteristics
YELLOW (C48330)
CAPSULE (C48336)
17 MM
IP;254
Product Packages
NDC Code 33261-202-00
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 33261-202-02
Package Description: 120 TABLET in 1 BOTTLE
NDC Code 33261-202-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 33261-202-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 33261-202-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 33261-202?
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".