NDC 21695-132 Tramadol Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 21695-132-00
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 21695-132-08
Package Description: 8 TABLET in 1 BOTTLE
NDC Code 21695-132-10
Package Description: 10 TABLET in 1 BOTTLE
NDC Code 21695-132-12
Package Description: 12 TABLET in 1 BOTTLE
NDC Code 21695-132-16
Package Description: 16 TABLET in 1 BOTTLE
NDC Code 21695-132-20
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 21695-132-21
Package Description: 21 TABLET in 1 BOTTLE
NDC Code 21695-132-24
Package Description: 24 TABLET in 1 BOTTLE
NDC Code 21695-132-28
Package Description: 28 TABLET in 1 BOTTLE
NDC Code 21695-132-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 21695-132-45
Package Description: 45 TABLET in 1 BOTTLE
NDC Code 21695-132-50
Package Description: 50 TABLET in 1 BOTTLE
NDC Code 21695-132-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 21695-132-64
Package Description: 240 TABLET in 1 BOTTLE
NDC Code 21695-132-72
Package Description: 120 TABLET in 1 BOTTLE
NDC Code 21695-132-78
Package Description: 180 TABLET in 1 BOTTLE
NDC Code 21695-132-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 21695-132?
What are the uses for Tramadol Hydrochloride?
Which are Tramadol Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRAMADOL HYDROCHLORIDE (UNII: 9N7R477WCK)
- TRAMADOL (UNII: 39J1LGJ30J) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Tramadol Hydrochloride?
- RxCUI: 835603 - traMADol HCl 50 MG Oral Tablet
- RxCUI: 835603 - tramadol hydrochloride 50 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".