Phentermine Hydrochloride

Product NDC
50436-6745
11-digit product format
504366745
Labeler code
50436
Product ID
50436-6745_671be0ff-6e88-43e3-917b-61100a21ffb0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Phentermine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Unit Dose Services
Application
ANDA040526
Marketing category
ANDA
Marketing start
2003-10-23
Marketing end
0000-00-00
Substance
PHENTERMINE HYDROCHLORIDE
Active strength
38 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
2019-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

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