Phendimetrazine Tartrate

Product NDC
68071-3040
11-digit product format
680713040
Labeler code
68071
Product ID
68071-3040_bb12c51c-4b2c-02c5-e053-2995a90ac05b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Phendimetrazine Tartrate
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
NDA018074
Marketing category
NDA
Marketing start
1977-09-06
Marketing end
0000-00-00
Substance
PHENDIMETRAZINE TARTRATE
Active strength
105 mg/1
Pharmacologic classes
Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]
DEA schedule
CIII
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68071-3040-16807130400114 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-3040-1) 2017-03-100000-00-00NoNoCurrent
68071-3040-36807130400330 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-3040-3) 2017-03-100000-00-00NoNoCurrent
68071-3040-86807130400828 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-3040-8) 2017-03-100000-00-00NoNoCurrent