Tramadol Hydrochloride

Product NDC
68788-8920
11-digit product format
687888920
Labeler code
68788
Product ID
68788-8920_9aa37e51-1c79-4043-a2f6-d1eaa7f0a5d4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Tramadol Hydrochloride
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
NDA022370
Marketing category
NDA
Marketing start
2015-09-18
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
68788-8920-3EA - Each68788-8920bd0fc792-54de-44c2-9c78-06f51eb01cea12019-08-06
68788-8920-6EA - Each68788-892075872992-8e0f-4996-b37d-b800a5b57da912019-08-06
68788-8920-9EA - Each68788-8920a9f5813a-bfe0-401e-a939-d934d201208112019-08-06