PHENDIMETRAZINE TARTRATE

Product NDC
43063-892
11-digit product format
430630892
Labeler code
43063
Product ID
43063-892_d0625fc9-2170-5d63-e053-2995a90abfaf
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
PHENDIMETRAZINE TARTRATE
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
NDA018074
Marketing category
NDA
Marketing start
2018-07-01
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
43063-892-14EA - Each43063-892937b91da-6085-4596-ae6d-d26a52b7784112018-10-11
43063-892-30EA - Each43063-89239bf2764-89a9-4fab-9f59-071de9549ab712018-10-11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
43063-892-144306308921414 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-892-14) 2018-09-050000-00-00NoNoCurrent
43063-892-304306308923030 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-892-30) 2018-09-200000-00-00NoNoCurrent