benzphetamine hydrochloride

Generic: benzphetamine hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benzphetamine hydrochloride
Generic Name benzphetamine hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

benzphetamine hydrochloride 50 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0451
Product ID 71335-0451_98aa03d7-8df0-4b01-8371-9761a0176afa
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 713350451
Hyphenated Format 71335-0451

Supplemental Identifiers

RxCUI
904368
UNII
43DWT87QT7

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
  • 30 TABLET in 1 BOTTLE (71335-0451-1)
  • 7 TABLET in 1 BOTTLE (71335-0451-2)
  • 14 TABLET in 1 BOTTLE (71335-0451-3)
  • 21 TABLET in 1 BOTTLE (71335-0451-4)
  • 42 TABLET in 1 BOTTLE (71335-0451-5)
  • 84 TABLET in 1 BOTTLE (71335-0451-6)
  • 60 TABLET in 1 BOTTLE (71335-0451-7)
  • 90 TABLET in 1 BOTTLE (71335-0451-8)
  • 120 TABLET in 1 BOTTLE (71335-0451-9)
source: ndc

Packages (9)

71335-0451-1 30 TABLET in 1 BOTTLE (71335-0451-1) 71335-0451-2 7 TABLET in 1 BOTTLE (71335-0451-2) 71335-0451-3 14 TABLET in 1 BOTTLE (71335-0451-3) 71335-0451-4 21 TABLET in 1 BOTTLE (71335-0451-4) 71335-0451-5 42 TABLET in 1 BOTTLE (71335-0451-5) 71335-0451-6 84 TABLET in 1 BOTTLE (71335-0451-6) 71335-0451-7 60 TABLET in 1 BOTTLE (71335-0451-7) 71335-0451-8 90 TABLET in 1 BOTTLE (71335-0451-8) 71335-0451-9 120 TABLET in 1 BOTTLE (71335-0451-9)

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": "98aa03d7-8df0-4b01-8371-9761a0176afa", "openfda": {"unii": ["43DWT87QT7"], "rxcui": ["904368"], "spl_set_id": ["1c726aa7-3b78-45de-aca0-fd8a5fff9403"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0451-1)", "package_ndc": "71335-0451-1", "marketing_start_date": "20180817"}, {"sample": false, "description": "7 TABLET in 1 BOTTLE (71335-0451-2)", "package_ndc": "71335-0451-2", "marketing_start_date": "20180725"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (71335-0451-3)", "package_ndc": "71335-0451-3", "marketing_start_date": "20180725"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (71335-0451-4)", "package_ndc": "71335-0451-4", "marketing_start_date": "20180914"}, {"sample": false, "description": "42 TABLET in 1 BOTTLE (71335-0451-5)", "package_ndc": "71335-0451-5", "marketing_start_date": "20180423"}, {"sample": false, "description": "84 TABLET in 1 BOTTLE (71335-0451-6)", "package_ndc": "71335-0451-6", "marketing_start_date": "20240529"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0451-7)", "package_ndc": "71335-0451-7", "marketing_start_date": "20180710"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0451-8)", "package_ndc": "71335-0451-8", "marketing_start_date": "20180212"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-0451-9)", "package_ndc": "71335-0451-9", "marketing_start_date": "20180529"}], "brand_name": "BENZPHETAMINE HYDROCHLORIDE", "product_id": "71335-0451_98aa03d7-8df0-4b01-8371-9761a0176afa", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "71335-0451", "dea_schedule": "CIII", "generic_name": "benzphetamine hydrochloride", "labeler_name": "Bryant Ranch Prepack", "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"}