Phentermine Hydrochloride

Product NDC
72789-287
11-digit product format
727890287
Labeler code
72789
Product ID
72789-287_3cf6a04a-fac4-c523-e063-6294a90a37ac
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
phentermine hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA205019
Marketing category
ANDA
Marketing start
2017-01-24
Substance
PHENTERMINE HYDROCHLORIDE
Active strength
30 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
72789-287-147278902871414 CAPSULE in 1 BOTTLE, PLASTIC (72789-287-14) 14 capsule2022-11-15NoNoHistorical
72789-287-287278902872828 CAPSULE in 1 BOTTLE, PLASTIC (72789-287-28) 28 capsule2025-05-07NoNoHistorical
72789-287-307278902873030 CAPSULE in 1 BOTTLE, PLASTIC (72789-287-30) 30 capsule2022-11-15NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Phentermine HydrochloridePD-Rx Pharmaceuticals, Inc.2025-08-22HUMAN PRESCRIPTION DRUG LABEL11