phendimetrazine tartrate

Generic: phendimetrazine tartrate

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

Drug Facts

Product Profile

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

phendimetrazine tartrate 35 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-3509
Product ID 68071-3509_23225e11-eb3a-d737-e063-6394a90ab811
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040762
DEA Schedule ciii
Listing Expiration 2026-12-31
Marketing Start 2012-11-20

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 680713509
Hyphenated Format 68071-3509

Supplemental Identifiers

RxCUI
979549
UPC
0368071350999
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 ANDA040762 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 35 mg/1
source: ndc
Packaging
  • 120 TABLET in 1 BOTTLE (68071-3509-1)
  • 60 TABLET in 1 BOTTLE (68071-3509-6)
  • 180 TABLET in 1 BOTTLE (68071-3509-8)
  • 90 TABLET in 1 BOTTLE (68071-3509-9)
source: ndc

Packages (4)

68071-3509-1 120 TABLET in 1 BOTTLE (68071-3509-1) 68071-3509-6 60 TABLET in 1 BOTTLE (68071-3509-6) 68071-3509-8 180 TABLET in 1 BOTTLE (68071-3509-8) 68071-3509-9 90 TABLET in 1 BOTTLE (68071-3509-9)

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": "23225e11-eb3a-d737-e063-6394a90ab811", "openfda": {"upc": ["0368071350999"], "unii": ["6985IP0T80"], "rxcui": ["979549"], "spl_set_id": ["05bb0569-4eed-2139-e063-6394a90acb6c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (68071-3509-1)", "package_ndc": "68071-3509-1", "marketing_start_date": "20240927"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3509-6)", "package_ndc": "68071-3509-6", "marketing_start_date": "20230919"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (68071-3509-8)", "package_ndc": "68071-3509-8", "marketing_start_date": "20240927"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3509-9)", "package_ndc": "68071-3509-9", "marketing_start_date": "20230919"}], "brand_name": "PHENDIMETRAZINE TARTRATE", "product_id": "68071-3509_23225e11-eb3a-d737-e063-6394a90ab811", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "68071-3509", "dea_schedule": "CIII", "generic_name": "Phendimetrazine Tartrate", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PHENDIMETRAZINE TARTRATE", "active_ingredients": [{"name": "PHENDIMETRAZINE TARTRATE", "strength": "35 mg/1"}], "application_number": "ANDA040762", "marketing_category": "ANDA", "marketing_start_date": "20121120", "listing_expiration_date": "20261231"}