phendimetrazine tartrate

Generic: phendimetrazine tartrate

Labeler: virtus pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phendimetrazine tartrate
Generic Name phendimetrazine tartrate
Labeler virtus pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phendimetrazine tartrate 35 mg/1

Manufacturer
Virtus Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69543-410
Product ID 69543-410_dc927d6a-f5b4-45e8-a732-c47831036d39
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA085588
DEA Schedule ciii
Listing Expiration 2026-12-31
Marketing Start 2018-07-01

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 69543410
Hyphenated Format 69543-410

Supplemental Identifiers

RxCUI
979549
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 ANDA085588 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 35 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (69543-410-10)
  • 1000 TABLET in 1 BOTTLE (69543-410-11)
source: ndc

Packages (2)

69543-410-10 100 TABLET in 1 BOTTLE (69543-410-10) 69543-410-11 1000 TABLET in 1 BOTTLE (69543-410-11)

Ingredients (1)

phendimetrazine tartrate (35 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": "dc927d6a-f5b4-45e8-a732-c47831036d39", "openfda": {"unii": ["6985IP0T80"], "rxcui": ["979549"], "spl_set_id": ["cc9a0cd2-6fb9-47ab-8e39-146d2fa361c2"], "manufacturer_name": ["Virtus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69543-410-10)", "package_ndc": "69543-410-10", "marketing_start_date": "20180701"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69543-410-11)", "package_ndc": "69543-410-11", "marketing_end_date": "20260930", "marketing_start_date": "20180701"}], "brand_name": "PHENDIMETRAZINE TARTRATE", "product_id": "69543-410_dc927d6a-f5b4-45e8-a732-c47831036d39", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "69543-410", "dea_schedule": "CIII", "generic_name": "PHENDIMETRAZINE TARTRATE", "labeler_name": "Virtus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PHENDIMETRAZINE TARTRATE", "active_ingredients": [{"name": "PHENDIMETRAZINE TARTRATE", "strength": "35 mg/1"}], "application_number": "ANDA085588", "marketing_category": "ANDA", "marketing_start_date": "20180701", "listing_expiration_date": "20261231"}