benzphetamine hydrochloride

Generic: benzphetamine hydrochloride

Labeler: epic pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benzphetamine hydrochloride
Generic Name benzphetamine hydrochloride
Labeler epic pharma, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

benzphetamine hydrochloride 50 mg/1

Manufacturer
Epic Pharma, LLC

Identifiers & Regulatory

Product NDC 42806-081
Product ID 42806-081_b4e5d191-8cbf-4111-a07b-025b920269c4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090346
DEA Schedule ciii
Listing Expiration 2026-12-31
Marketing Start 2015-12-16

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 42806081
Hyphenated Format 42806-081

Supplemental Identifiers

RxCUI
904368
UPC
0342806081013
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 ANDA090346 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (42806-081-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (42806-081-05)
  • 30 TABLET, FILM COATED in 1 BOTTLE (42806-081-30)
source: ndc

Packages (3)

42806-081-01 100 TABLET, FILM COATED in 1 BOTTLE (42806-081-01) 42806-081-05 500 TABLET, FILM COATED in 1 BOTTLE (42806-081-05) 42806-081-30 30 TABLET, FILM COATED in 1 BOTTLE (42806-081-30)

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": "b4e5d191-8cbf-4111-a07b-025b920269c4", "openfda": {"upc": ["0342806081013"], "unii": ["43DWT87QT7"], "rxcui": ["904368"], "spl_set_id": ["f6d9b369-4b64-4d3f-844d-5d60dd257c55"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (42806-081-01)", "package_ndc": "42806-081-01", "marketing_start_date": "20151216"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (42806-081-05)", "package_ndc": "42806-081-05", "marketing_start_date": "20151216"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42806-081-30)", "package_ndc": "42806-081-30", "marketing_start_date": "20151216"}], "brand_name": "Benzphetamine Hydrochloride", "product_id": "42806-081_b4e5d191-8cbf-4111-a07b-025b920269c4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "42806-081", "dea_schedule": "CIII", "generic_name": "Benzphetamine Hydrochloride", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benzphetamine Hydrochloride", "active_ingredients": [{"name": "BENZPHETAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA090346", "marketing_category": "ANDA", "marketing_start_date": "20151216", "listing_expiration_date": "20261231"}