tramadol hydrochloride

Product NDC
55700-864
11-digit product format
557000864
Labeler code
55700
Product ID
55700-864_e9e9c8cd-c2ee-4e92-8665-466dcc5c2a29
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
tramadol hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Quality Care Products, LLC
Application
ANDA075964
Marketing category
ANDA
Marketing start
2020-09-25
Marketing end
0000-00-00
Substance
TRAMADOL HYDROCHLORIDE
Active strength
50 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55700-864-0155700086401120 TABLET in 1 BOTTLE (55700-864-01) 120 tablet2020-09-250000-00-00NoNoCurrent
55700-864-155570008641515 TABLET in 1 BOTTLE (55700-864-15) 15 tablet2020-09-250000-00-00NoNoCurrent
55700-864-1855700086418180 TABLET in 1 BOTTLE (55700-864-18) 180 tablet2020-09-250000-00-00NoNoCurrent
55700-864-2455700086424240 TABLET in 1 BOTTLE (55700-864-24) 240 tablet2020-09-250000-00-00NoNoCurrent
55700-864-305570008643030 TABLET in 1 BOTTLE (55700-864-30) 30 tablet2020-09-250000-00-00NoNoCurrent
55700-864-605570008646060 TABLET in 1 BOTTLE (55700-864-60) 60 tablet2020-09-250000-00-00NoNoCurrent
55700-864-905570008649090 TABLET in 1 BOTTLE (55700-864-90) 90 tablet2020-09-250000-00-00NoNoCurrent