phendimetrazine tartrate

Generic: phendimetrazine tartrate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phendimetrazine tartrate
Generic Name phendimetrazine tartrate
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phendimetrazine tartrate 35 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-0715
Product ID 50090-0715_04c270db-a517-4b1a-a6b9-b1eda68fcc7b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091042
DEA Schedule ciii
Listing Expiration 2026-12-31
Marketing Start 2010-09-15

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 500900715
Hyphenated Format 50090-0715

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
  • 30 TABLET in 1 BOTTLE (50090-0715-0)
  • 60 TABLET in 1 BOTTLE (50090-0715-1)
  • 90 TABLET in 1 BOTTLE (50090-0715-2)
  • 28 TABLET in 1 BOTTLE (50090-0715-6)
source: ndc

Packages (4)

50090-0715-0 30 TABLET in 1 BOTTLE (50090-0715-0) 50090-0715-1 60 TABLET in 1 BOTTLE (50090-0715-1) 50090-0715-2 90 TABLET in 1 BOTTLE (50090-0715-2) 50090-0715-6 28 TABLET in 1 BOTTLE (50090-0715-6)

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": "04c270db-a517-4b1a-a6b9-b1eda68fcc7b", "openfda": {"unii": ["6985IP0T80"], "rxcui": ["979549"], "spl_set_id": ["f1d265e1-522e-4a62-afda-29477fb94b8d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-0715-0)", "package_ndc": "50090-0715-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-0715-1)", "package_ndc": "50090-0715-1", "marketing_start_date": "20141128"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-0715-2)", "package_ndc": "50090-0715-2", "marketing_start_date": "20141128"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (50090-0715-6)", "package_ndc": "50090-0715-6", "marketing_start_date": "20141128"}], "brand_name": "Phendimetrazine Tartrate", "product_id": "50090-0715_04c270db-a517-4b1a-a6b9-b1eda68fcc7b", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "50090-0715", "dea_schedule": "CIII", "generic_name": "Phendimetrazine Tartrate", "labeler_name": "A-S Medication Solutions", "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": "20100915", "listing_expiration_date": "20261231"}