phendimetrazine tartrate

Generic: phendimetrazine tartrate

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phendimetrazine tartrate
Generic Name phendimetrazine tartrate
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phendimetrazine tartrate 35 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7236
Product ID 68788-7236_52c5af94-7c7f-44b6-9c85-ec964ce4c136
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091042
DEA Schedule ciii
Listing Expiration 2026-12-31
Marketing Start 2018-08-13

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 687887236
Hyphenated Format 68788-7236

Supplemental Identifiers

RxCUI
979549
UNII
6985IP0T80

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 ANDA091042 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 35 mg/1
source: ndc
Packaging
  • 14 TABLET in 1 BOTTLE (68788-7236-1)
  • 28 TABLET in 1 BOTTLE (68788-7236-2)
  • 30 TABLET in 1 BOTTLE (68788-7236-3)
  • 7 TABLET in 1 BOTTLE (68788-7236-7)
source: ndc

Packages (4)

68788-7236-1 14 TABLET in 1 BOTTLE (68788-7236-1) 68788-7236-2 28 TABLET in 1 BOTTLE (68788-7236-2) 68788-7236-3 30 TABLET in 1 BOTTLE (68788-7236-3) 68788-7236-7 7 TABLET in 1 BOTTLE (68788-7236-7)

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": "52c5af94-7c7f-44b6-9c85-ec964ce4c136", "openfda": {"unii": ["6985IP0T80"], "rxcui": ["979549"], "spl_set_id": ["767b5386-1e56-4eeb-8d59-510b940ab75e"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE (68788-7236-1)", "package_ndc": "68788-7236-1", "marketing_start_date": "20180813"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (68788-7236-2)", "package_ndc": "68788-7236-2", "marketing_start_date": "20180813"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7236-3)", "package_ndc": "68788-7236-3", "marketing_start_date": "20180813"}, {"sample": false, "description": "7 TABLET in 1 BOTTLE (68788-7236-7)", "package_ndc": "68788-7236-7", "marketing_start_date": "20180813"}], "brand_name": "Phendimetrazine Tartrate", "product_id": "68788-7236_52c5af94-7c7f-44b6-9c85-ec964ce4c136", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "68788-7236", "dea_schedule": "CIII", "generic_name": "Phendimetrazine Tartrate", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phendimetrazine Tartrate", "active_ingredients": [{"name": "PHENDIMETRAZINE TARTRATE", "strength": "35 mg/1"}], "application_number": "ANDA091042", "marketing_category": "ANDA", "marketing_start_date": "20180813", "listing_expiration_date": "20261231"}