Tramadol Hydrochloride

Product NDC
63187-062
11-digit product format
631870062
Labeler code
63187
Product ID
63187-062_6913b786-94ec-4e2f-bc5b-4b8b796b9b8a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Tramadol Hydrochloride
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
Proficient Rx LP
Application
NDA022370
Marketing category
NDA
Marketing start
2012-03-14
Marketing end
0000-00-00
Substance
TRAMADOL HYDROCHLORIDE
Active strength
150 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63187-062-30EA - Each63187-0628589895d-bb4d-498d-9404-46084323a81412016-06-14
63187-062-60EA - Each63187-0628815721c-e1e3-4fd5-9a2e-953cdd5162c412015-11-12