Phentermine Hydrochloride

Product NDC
71205-564
11-digit product format
712050564
Labeler code
71205
Product ID
71205-564_39d7a8f2-00e7-4629-8e93-7175f047e331
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
phentermine hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA205019
Marketing category
ANDA
Marketing start
2017-01-24
Substance
PHENTERMINE HYDROCHLORIDE
Active strength
15 mg/1
Pharmacologic classes
Appetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
0K2I505OTVPHENTERMINE HYDROCHLORIDE1197-21-3PHENTERMINE HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71205-564-07712050564077 CAPSULE in 1 BOTTLE (71205-564-07) 7 capsule2021-05-10NoNoHistorical
71205-564-157120505641515 CAPSULE in 1 BOTTLE (71205-564-15) 15 capsule2021-05-10NoNoHistorical
71205-564-307120505643030 CAPSULE in 1 BOTTLE (71205-564-30) 30 capsule2021-05-10NoNoHistorical
71205-564-607120505646060 CAPSULE in 1 BOTTLE (71205-564-60) 60 capsule2021-05-10NoNoHistorical
71205-564-907120505649090 CAPSULE in 1 BOTTLE (71205-564-90) 90 capsule2021-05-10NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Phentermine HydrochlorideProficient Rx LP2022-03-01HUMAN PRESCRIPTION DRUG LABEL2