phendimetrazine tartrate

Generic: phendimetrazine tartrate

Labeler: acertis pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name phendimetrazine tartrate
Generic Name phendimetrazine tartrate
Labeler acertis pharmaceuticals, llc
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

phendimetrazine tartrate 105 mg/1

Manufacturer
Acertis Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 72989-409
Product ID 72989-409_72552285-ab14-4e9f-957a-d913b31bdd84
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018074
DEA Schedule ciii
Listing Expiration 2026-12-31
Marketing Start 2022-11-01

Pharmacologic Class

Classes
appetite suppression [pe] increased sympathetic activity [pe] sympathomimetic amine anorectic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72989409
Hyphenated Format 72989-409

Supplemental Identifiers

RxCUI
979543
UPC
0372989409304
UNII
6985IP0T80

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name phendimetrazine tartrate (source: ndc)
Generic Name phendimetrazine tartrate (source: ndc)
Application Number NDA018074 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 105 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72989-409-30)
source: ndc

Packages (1)

72989-409-30 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72989-409-30)

Ingredients (1)

phendimetrazine tartrate (105 mg/1)

Linked Drug Pages (1)

PHENDIMETRAZINE TARTRATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "72552285-ab14-4e9f-957a-d913b31bdd84", "openfda": {"upc": ["0372989409304"], "unii": ["6985IP0T80"], "rxcui": ["979543"], "spl_set_id": ["162140d3-b833-4633-9759-95821a46a690"], "manufacturer_name": ["Acertis Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72989-409-30)", "package_ndc": "72989-409-30", "marketing_start_date": "20221101"}], "brand_name": "PHENDIMETRAZINE TARTRATE", "product_id": "72989-409_72552285-ab14-4e9f-957a-d913b31bdd84", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "72989-409", "dea_schedule": "CIII", "generic_name": "PHENDIMETRAZINE TARTRATE", "labeler_name": "Acertis Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PHENDIMETRAZINE TARTRATE", "active_ingredients": [{"name": "PHENDIMETRAZINE TARTRATE", "strength": "105 mg/1"}], "application_number": "NDA018074", "marketing_category": "NDA", "marketing_start_date": "20221101", "listing_expiration_date": "20261231"}