NDC 21695-132 Tramadol Hydrochloride

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
21695-132
Proprietary Name:
Tramadol Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rebel Distributors Corp.
Labeler Code:
21695
Start Marketing Date: [9]
11-23-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
9 MM
Imprint(s):
AN;627
Score:
1

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?

The NDC code 21695-132 is assigned by the FDA to the product Tramadol Hydrochloride which is product labeled by Rebel Distributors Corp.. The product's dosage form is . The product is distributed in 17 packages with assigned NDC codes 21695-132-00 100 tablet in 1 bottle , 21695-132-08 8 tablet in 1 bottle , 21695-132-10 10 tablet in 1 bottle , 21695-132-12 12 tablet in 1 bottle , 21695-132-16 16 tablet in 1 bottle , 21695-132-20 20 tablet in 1 bottle , 21695-132-21 21 tablet in 1 bottle , 21695-132-24 24 tablet in 1 bottle , 21695-132-28 28 tablet in 1 bottle , 21695-132-30 30 tablet in 1 bottle , 21695-132-45 45 tablet in 1 bottle , 21695-132-50 50 tablet in 1 bottle , 21695-132-60 60 tablet in 1 bottle , 21695-132-64 240 tablet in 1 bottle , 21695-132-72 120 tablet in 1 bottle , 21695-132-78 180 tablet in 1 bottle , 21695-132-90 90 tablet in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Tramadol Hydrochloride?

Tramadol hydrochloride is indicated for the management of moderate to moderately severe pain in adults.

Which are Tramadol Hydrochloride UNII Codes?

The UNII codes for the active ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Tramadol Hydrochloride?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* Please review the disclaimer below.

Product Footnotes

[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".