Phentermine Hydrochloride

Product NDC
49999-517
11-digit product format
499990517
Labeler code
49999
Product ID
49999-517_50c79990-4609-4b6b-8b74-ccc0231a63f8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Phentermine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products
Application
ANDA040876
Marketing category
ANDA
Marketing start
2012-08-15
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
2020-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

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