phendimetrazine tartrate

Generic: phendimetrazine tartrate

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phendimetrazine tartrate
Generic Name phendimetrazine tartrate
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phendimetrazine tartrate 35 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-510
Product ID 43063-510_2b33c59d-56f9-8ed2-e063-6394a90a1ad6
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 43063510
Hyphenated Format 43063-510

Supplemental Identifiers

RxCUI
979549
UPC
0343063510568
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
  • 7 TABLET in 1 BOTTLE, PLASTIC (43063-510-07)
  • 14 TABLET in 1 BOTTLE, PLASTIC (43063-510-14)
  • 28 TABLET in 1 BOTTLE, PLASTIC (43063-510-28)
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-510-30)
  • 42 TABLET in 1 BOTTLE, PLASTIC (43063-510-42)
  • 56 TABLET in 1 BOTTLE, PLASTIC (43063-510-56)
  • 60 TABLET in 1 BOTTLE, PLASTIC (43063-510-60)
  • 135 TABLET in 1 BOTTLE, PLASTIC (43063-510-81)
  • 112 TABLET in 1 BOTTLE, PLASTIC (43063-510-88)
  • 90 TABLET in 1 BOTTLE, PLASTIC (43063-510-90)
source: ndc

Packages (10)

Ingredients (1)

phendimetrazine tartrate (35 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b33c59d-56f9-8ed2-e063-6394a90a1ad6", "openfda": {"upc": ["0343063510568"], "unii": ["6985IP0T80"], "rxcui": ["979549"], "spl_set_id": ["467ae7d7-e342-423b-be89-5d38c1abf3c9"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET in 1 BOTTLE, PLASTIC (43063-510-07)", "package_ndc": "43063-510-07", "marketing_start_date": "20170623"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (43063-510-14)", "package_ndc": "43063-510-14", "marketing_start_date": "20170411"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE, PLASTIC (43063-510-28)", "package_ndc": "43063-510-28", "marketing_start_date": "20100915"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-510-30)", "package_ndc": "43063-510-30", "marketing_start_date": "20100915"}, {"sample": false, "description": "42 TABLET in 1 BOTTLE, PLASTIC (43063-510-42)", "package_ndc": "43063-510-42", "marketing_start_date": "20231006"}, {"sample": false, "description": "56 TABLET in 1 BOTTLE, PLASTIC (43063-510-56)", "package_ndc": "43063-510-56", "marketing_start_date": "20170623"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-510-60)", "package_ndc": "43063-510-60", "marketing_start_date": "20100915"}, {"sample": false, "description": "135 TABLET in 1 BOTTLE, PLASTIC (43063-510-81)", "package_ndc": "43063-510-81", "marketing_start_date": "20180501"}, {"sample": false, "description": "112 TABLET in 1 BOTTLE, PLASTIC (43063-510-88)", "package_ndc": "43063-510-88", "marketing_start_date": "20170419"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-510-90)", "package_ndc": "43063-510-90", "marketing_start_date": "20170419"}], "brand_name": "Phendimetrazine Tartrate", "product_id": "43063-510_2b33c59d-56f9-8ed2-e063-6394a90a1ad6", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "43063-510", "dea_schedule": "CIII", "generic_name": "Phendimetrazine Tartrate", "labeler_name": "PD-Rx 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": "20100915", "listing_expiration_date": "20261231"}