phendimetrazine tartrate

Generic: phendimetrazine tartrate

Labeler: kvk-tech, inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phendimetrazine tartrate
Generic Name phendimetrazine tartrate
Labeler kvk-tech, inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phendimetrazine tartrate 35 mg/1

Manufacturer
KVK-TECH, INC

Identifiers & Regulatory

Product NDC 10702-045
Product ID 10702-045_289ebb0b-370d-4ea1-e063-6394a90a1752
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 10702045
Hyphenated Format 10702-045

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 ANDA091042 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 35 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (10702-045-01)
  • 30 TABLET in 1 BOTTLE (10702-045-03)
  • 1000 TABLET in 1 BOTTLE (10702-045-10)
source: ndc

Packages (3)

10702-045-01 100 TABLET in 1 BOTTLE (10702-045-01) 10702-045-03 30 TABLET in 1 BOTTLE (10702-045-03) 10702-045-10 1000 TABLET in 1 BOTTLE (10702-045-10)

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": "289ebb0b-370d-4ea1-e063-6394a90a1752", "openfda": {"unii": ["6985IP0T80"], "rxcui": ["979549"], "spl_set_id": ["07bf3488-09e7-436f-af3f-94c35a7be025"], "manufacturer_name": ["KVK-TECH, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-045-01)", "package_ndc": "10702-045-01", "marketing_start_date": "20100915"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (10702-045-03)", "package_ndc": "10702-045-03", "marketing_start_date": "20100915"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (10702-045-10)", "package_ndc": "10702-045-10", "marketing_start_date": "20100915"}], "brand_name": "Phendimetrazine Tartrate", "product_id": "10702-045_289ebb0b-370d-4ea1-e063-6394a90a1752", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "10702-045", "dea_schedule": "CIII", "generic_name": "Phendimetrazine Tartrate", "labeler_name": "KVK-TECH, 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"}