benzphetamine hydrochloride

Generic: benzphetamine hydrochloride

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

Drug Facts

Product Profile

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

benzphetamine hydrochloride 50 mg/1

Manufacturer
KVK-TECH, INC

Identifiers & Regulatory

Product NDC 10702-040
Product ID 10702-040_15d75638-8ac7-e610-e063-6394a90af99c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090968
DEA Schedule ciii
Listing Expiration 2026-12-31
Marketing Start 2010-07-21

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 10702040
Hyphenated Format 10702-040

Supplemental Identifiers

RxCUI
904368
UNII
43DWT87QT7

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 benzphetamine hydrochloride (source: ndc)
Generic Name benzphetamine hydrochloride (source: ndc)
Application Number ANDA090968 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (10702-040-01)
  • 30 TABLET in 1 BOTTLE (10702-040-03)
  • 1000 TABLET in 1 BOTTLE (10702-040-10)
  • 500 TABLET in 1 BOTTLE (10702-040-50)
source: ndc

Packages (4)

10702-040-01 100 TABLET in 1 BOTTLE (10702-040-01) 10702-040-03 30 TABLET in 1 BOTTLE (10702-040-03) 10702-040-10 1000 TABLET in 1 BOTTLE (10702-040-10) 10702-040-50 500 TABLET in 1 BOTTLE (10702-040-50)

Ingredients (1)

benzphetamine hydrochloride (50 mg/1)

Linked Drug Pages (1)

BENZPHETAMINE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "15d75638-8ac7-e610-e063-6394a90af99c", "openfda": {"unii": ["43DWT87QT7"], "rxcui": ["904368"], "spl_set_id": ["14d4589d-7f1c-4b6e-9557-59dad39b0960"], "manufacturer_name": ["KVK-TECH, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-040-01)", "package_ndc": "10702-040-01", "marketing_start_date": "20100721"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (10702-040-03)", "package_ndc": "10702-040-03", "marketing_start_date": "20100721"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (10702-040-10)", "package_ndc": "10702-040-10", "marketing_start_date": "20100721"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (10702-040-50)", "package_ndc": "10702-040-50", "marketing_start_date": "20100721"}], "brand_name": "BENZPHETAMINE HYDROCHLORIDE", "product_id": "10702-040_15d75638-8ac7-e610-e063-6394a90af99c", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "10702-040", "dea_schedule": "CIII", "generic_name": "benzphetamine hydrochloride", "labeler_name": "KVK-TECH, INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BENZPHETAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "BENZPHETAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA090968", "marketing_category": "ANDA", "marketing_start_date": "20100721", "listing_expiration_date": "20261231"}