Phentermine Hydrochloride

Product NDC
71205-785
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
phentermine hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA205019
Marketing category
ANDA
Substance
PHENTERMINE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
71205-785-3030 CAPSULE in 1 BOTTLE (71205-785-30) 2023-04-03NoHistorical
71205-785-6060 CAPSULE in 1 BOTTLE (71205-785-60) 2023-04-03NoHistorical
71205-785-9090 CAPSULE in 1 BOTTLE (71205-785-90) 2023-04-03NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Phentermine HydrochlorideProficient Rx LP2023-04-01HUMAN PRESCRIPTION DRUG LABEL1