phentermine hydrochloride

Product NDC
50436-9028
11-digit product format
504369028
Labeler code
50436
Product ID
50436-9028_d761706f-1f5b-4f11-be5c-7e88eb360fa9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
phentermine hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Unit Dose Services
Application
ANDA087190
Marketing category
ANDA
Marketing start
1981-06-12
Marketing end
0000-00-00
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
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50436-9028-1EA - Each50436-9028507b8c8b-c5d0-4135-8606-550225f1513c12013-03-03