Tramadol Hydrochloride

Product NDC
55700-293
11-digit product format
557000293
Labeler code
55700
Product ID
55700-293_ae7cabc3-e9f3-448b-b5a0-230fee8c19a3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Tramadol Hydrochloride
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
NDA022370
Marketing category
NDA
Marketing start
2015-07-01
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

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-293-15EA - Each55700-293660f64be-aa69-4535-9635-90706982f37b12017-12-14
55700-293-30EA - Each55700-293a5c8b8a8-66ce-4067-96e3-97cfce6112e412017-12-14
55700-293-60EA - Each55700-2938b8afe5e-fbf7-4234-a8c2-cbad11cf3c5912017-12-14
55700-293-90EA - Each55700-293ab7bccc6-1ecf-446f-b529-58b9545b414e12017-12-14