Phentermine Hydrochloride

Product NDC
55289-701
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Phentermine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA040876
Marketing category
ANDA
Substance
PHENTERMINE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
55289-701-077 TABLET in 1 BOTTLE, PLASTIC (55289-701-07) 2015-09-29NoHistorical
55289-701-1414 TABLET in 1 BOTTLE, PLASTIC (55289-701-14) 2015-09-29NoHistorical
55289-701-1515 TABLET in 1 BOTTLE, PLASTIC (55289-701-15) 2015-09-29NoHistorical
55289-701-2121 TABLET in 1 BOTTLE, PLASTIC (55289-701-21) 2015-09-29NoHistorical
55289-701-2828 TABLET in 1 BOTTLE, PLASTIC (55289-701-28) 2015-09-29NoHistorical
55289-701-3030 TABLET in 1 BOTTLE, PLASTIC (55289-701-30) 2015-09-29NoHistorical
55289-701-3232 TABLET in 1 BOTTLE, PLASTIC (55289-701-32) 2015-09-29NoHistorical
55289-701-4242 TABLET in 1 BOTTLE, PLASTIC (55289-701-42) 2016-12-15NoHistorical
55289-701-4545 TABLET in 1 BOTTLE, PLASTIC (55289-701-45) 2015-09-29NoHistorical
55289-701-5656 TABLET in 1 BOTTLE, PLASTIC (55289-701-56) 2016-10-24NoHistorical
55289-701-6060 TABLET in 1 BOTTLE, PLASTIC (55289-701-60) 2015-09-29NoHistorical
55289-701-9090 TABLET in 1 BOTTLE, PLASTIC (55289-701-90) 2015-09-29NoHistorical
55289-701-98120 TABLET in 1 BOTTLE, PLASTIC (55289-701-98) 2016-12-15NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Phentermine HydrochloridePD-Rx Pharmaceuticals, Inc.2025-10-20HUMAN PRESCRIPTION DRUG LABEL20
Phentermine HydrochloridePD-Rx Pharmaceuticals, Inc.2024-03-12HUMAN PRESCRIPTION DRUG LABEL19