Home NDC 63629-3051-7 Phendimetrazine Tartrate
Product NDC 63629-3051
Requested package NDC 63629-3051-7
11-digit product format 636293051
Labeler code 63629
Product ID 63629-3051_73ea77b3-ac38-4888-9e19-74b2f5e6887f
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Phendimetrazine Tartrate
Dosage form CAPSULE, EXTENDED RELEASE
Route ORAL
Labeler Bryant Ranch Prepack
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 2021-12-31
Current FDA listing Historical FDA.report record Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N018074-001 PHENDIMETRAZINE TARTRATE PHENDIMETRAZINE TARTRATE 105MG CAPSULE, EXTENDED RELEASE / ORAL RLD, RS, Approved before 1982
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-08-01 22:54:32 2026-06 N018074-001 PHENDIMETRAZINE TARTRATE 105MG CAPSULE, EXTENDED RELEASE / ORAL RLD, RS, Approved before 1982 a50c72e98297…
openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded PHENDIMETRAZINE TARTRATE ACTIVE INGREDIENT 6985IP0T80 PHENDIMETRAZINE TARTRATE CAPSULE, EXTENDED RELEASE [BRYANT RANCH PREPACK] 2 PHENDIMETRAZINE ACTIVE MOIETY AB2794W8KV PHENDIMETRAZINE TARTRATE CAPSULE, EXTENDED RELEASE [BRYANT RANCH PREPACK] 2 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD PHENDIMETRAZINE TARTRATE CAPSULE, EXTENDED RELEASE [BRYANT RANCH PREPACK] 2 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA PHENDIMETRAZINE TARTRATE CAPSULE, EXTENDED RELEASE [BRYANT RANCH PREPACK] 2 GELATIN INACTIVE INGREDIENT 2G86QN327L PHENDIMETRAZINE TARTRATE CAPSULE, EXTENDED RELEASE [BRYANT RANCH PREPACK] 2 POVIDONES INACTIVE INGREDIENT FZ989GH94E PHENDIMETRAZINE TARTRATE CAPSULE, EXTENDED RELEASE [BRYANT RANCH PREPACK] 2 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 PHENDIMETRAZINE TARTRATE CAPSULE, EXTENDED RELEASE [BRYANT RANCH PREPACK] 2 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J PHENDIMETRAZINE TARTRATE CAPSULE, EXTENDED RELEASE [BRYANT RANCH PREPACK] 2 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ PHENDIMETRAZINE TARTRATE CAPSULE, EXTENDED RELEASE [BRYANT RANCH PREPACK] 2 SUCROSE INACTIVE INGREDIENT C151H8M554 PHENDIMETRAZINE TARTRATE CAPSULE, EXTENDED RELEASE [BRYANT RANCH PREPACK] 2 TALC INACTIVE INGREDIENT 7SEV7J4R1U PHENDIMETRAZINE TARTRATE CAPSULE, EXTENDED RELEASE [BRYANT RANCH PREPACK] 2
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 63629-3051-7 63629305107 14 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-3051-7) 2008-11-20 0000-00-00 No No Current