Tramadol Hydrochloride and Acetaminophen

Product NDC
55700-124
11-digit product format
557000124
Labeler code
55700
Product ID
55700-124_3b5a123e-22ea-4220-86a5-95ad7c9a9df1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Tramadol Hydrochloride and Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA090485
Marketing category
ANDA
Marketing start
2009-12-17
Marketing end
0000-00-00
Substance
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN
Active strength
38 mg/1; 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
55700-124-30EA - Each55700-124c0f047eb-596a-45e0-91c3-3908c75ba7a512017-12-14
55700-124-60EA - Each55700-1248127aa4a-57f8-4514-ae99-8b0da01b8b9e12017-12-14