12634-786 NDC - TRAMADOL HYDROCHLORIDE ()

Drug Information

Product NDC: 12634-786

Proprietary Name: TRAMADOL HYDROCHLORIDE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: APOTHECA, INC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/15/2010

Package Information

No. Package Code Package Description Billing Unit
112634-786-0010 TABLET in 1 BOTTLE (12634-786-00)
212634-786-01100 TABLET in 1 BOTTLE (12634-786-01)
312634-786-5050 TABLET in 1 BOTTLE (12634-786-50)
412634-786-5212 TABLET in 1 BLISTER PACK (12634-786-52)
512634-786-5414 TABLET in 1 BLISTER PACK (12634-786-54)
612634-786-5515 TABLET in 1 BLISTER PACK (12634-786-55)
712634-786-5720 TABLET in 1 BLISTER PACK (12634-786-57)
812634-786-5930 TABLET in 1 BLISTER PACK (12634-786-59)
912634-786-6060 TABLET in 1 BOTTLE (12634-786-60)EA
1012634-786-6110 TABLET in 1 BLISTER PACK (12634-786-61)
1112634-786-622 TABLET in 1 BLISTER PACK (12634-786-62)
1212634-786-655 TABLET in 1 BLISTER PACK (12634-786-65)
1312634-786-666 TABLET in 1 BLISTER PACK (12634-786-66)
1412634-786-7130 TABLET in 1 BOTTLE (12634-786-71)EA
1512634-786-7925 TABLET in 1 BOTTLE (12634-786-79)
1612634-786-8020 TABLET in 1 BOTTLE (12634-786-80)EA
1712634-786-8121 TABLET in 1 BOTTLE (12634-786-81)
1812634-786-8515 TABLET in 1 BOTTLE (12634-786-85)
1912634-786-9090 TABLET in 1 BOTTLE (12634-786-90)
2012634-786-911 TABLET in 1 BLISTER PACK (12634-786-91)
2112634-786-966 TABLET in 1 BOTTLE (12634-786-96)

NDC Record

Field Name Field Value Definition
PRODUCT NDC12634-786The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMETRAMADOL HYDROCHLORIDEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/15/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAPOTHECA, INCName of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 2/1/2023