diethylpropion hydrochloride

Generic: diethylpropion hydrochloride

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

Drug Facts

Product Profile

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

diethylpropion hydrochloride 25 mg/1

Manufacturer
KVK-TECH, INC

Identifiers & Regulatory

Product NDC 10702-044
Product ID 10702-044_1764f49c-0f71-0bfc-e063-6294a90a8a48
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201212
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2010-12-27

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 10702044
Hyphenated Format 10702-044

Supplemental Identifiers

RxCUI
978654
UNII
19V2PL39NG

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 diethylpropion hydrochloride (source: ndc)
Generic Name diethylpropion hydrochloride (source: ndc)
Application Number ANDA201212 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (10702-044-01)
  • 30 TABLET in 1 BOTTLE (10702-044-03)
  • 60 TABLET in 1 BOTTLE (10702-044-06)
source: ndc

Packages (3)

10702-044-01 100 TABLET in 1 BOTTLE (10702-044-01) 10702-044-03 30 TABLET in 1 BOTTLE (10702-044-03) 10702-044-06 60 TABLET in 1 BOTTLE (10702-044-06)

Ingredients (1)

diethylpropion hydrochloride (25 mg/1)

Linked Drug Pages (1)

DIETHYLPROPION HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1764f49c-0f71-0bfc-e063-6294a90a8a48", "openfda": {"unii": ["19V2PL39NG"], "rxcui": ["978654"], "spl_set_id": ["3ecb7bd7-e04c-47fe-859a-8ba8a54f9aff"], "manufacturer_name": ["KVK-TECH, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-044-01)", "package_ndc": "10702-044-01", "marketing_start_date": "20101227"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (10702-044-03)", "package_ndc": "10702-044-03", "marketing_start_date": "20101227"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (10702-044-06)", "package_ndc": "10702-044-06", "marketing_start_date": "20101227"}], "brand_name": "DIETHYLPROPION HYDROCHLORIDE", "product_id": "10702-044_1764f49c-0f71-0bfc-e063-6294a90a8a48", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "10702-044", "dea_schedule": "CIV", "generic_name": "DIETHYLPROPION HYDROCHLORIDE", "labeler_name": "KVK-TECH, INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIETHYLPROPION HYDROCHLORIDE", "active_ingredients": [{"name": "DIETHYLPROPION HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA201212", "marketing_category": "ANDA", "marketing_start_date": "20101227", "listing_expiration_date": "20261231"}