tramadol hydrochloride

Product NDC
82804-114
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
tramadol hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA202075
Marketing category
ANDA
Substance
TRAMADOL HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
82804-114-1515 TABLET in 1 BOTTLE (82804-114-15) 2024-07-02NoHistorical
82804-114-2020 TABLET in 1 BOTTLE (82804-114-20) 2024-07-02NoHistorical
82804-114-3030 TABLET in 1 BOTTLE (82804-114-30) 2024-07-02NoHistorical
82804-114-4040 TABLET in 1 BOTTLE (82804-114-40) 2024-07-02NoHistorical
82804-114-6060 TABLET in 1 BOTTLE (82804-114-60) 2024-07-02NoHistorical
82804-114-64240 TABLET in 1 BOTTLE (82804-114-64) 2024-07-02NoHistorical
82804-114-72120 TABLET in 1 BOTTLE (82804-114-72) 2024-07-02NoHistorical
82804-114-78180 TABLET in 1 BOTTLE (82804-114-78) 2024-07-02NoHistorical
82804-114-9090 TABLET in 1 BOTTLE (82804-114-90) 2024-07-02NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
tramadol hydrochlorideProficient Rx LP2024-07-01HUMAN PRESCRIPTION DRUG LABEL1