Tramadol Hydrochloride

Product NDC
67046-730
11-digit product format
670460730
Labeler code
67046
Product ID
67046-730_a1527d3b-85a5-4588-8ce3-533ecb48ab7f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Tramadol Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Contract Pharmacy Services-PA
Application
ANDA076003
Marketing category
ANDA
Marketing start
2010-02-26
Marketing end
0000-00-00
Substance
TRAMADOL HYDROCHLORIDE
Active strength
50 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA],Opioid Agonist [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
9N7R477WCKTRAMADOL HYDROCHLORIDE36282-47-0TRAMADOL HYDROCHLORIDE

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Tramadol Hydrochloride TabletsContract Pharmacy Services-PA2010-08-17HUMAN PRESCRIPTION DRUG LABEL2