benzphetamine hydrochloride

Generic: benzphetamine hydrochloride

Labeler: calvin scott & co., inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benzphetamine hydrochloride
Generic Name benzphetamine hydrochloride
Labeler calvin scott & co., inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

benzphetamine hydrochloride 50 mg/1

Manufacturer
Calvin Scott & Co., Inc.

Identifiers & Regulatory

Product NDC 17224-672
Product ID 17224-672_f5ee265f-9765-de77-e053-2a95a90ac76f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090968
DEA Schedule ciii
Listing Expiration 2026-12-31
Marketing Start 2010-01-01

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 17224672
Hyphenated Format 17224-672

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, PLASTIC (17224-672-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (17224-672-60)
source: ndc

Packages (2)

17224-672-30 30 TABLET in 1 BOTTLE, PLASTIC (17224-672-30) 17224-672-60 60 TABLET in 1 BOTTLE, PLASTIC (17224-672-60)

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": "f5ee265f-9765-de77-e053-2a95a90ac76f", "openfda": {"unii": ["43DWT87QT7"], "rxcui": ["904368"], "spl_set_id": ["f5c3c2ed-54a2-1def-e053-2995a90ab4e3"], "manufacturer_name": ["Calvin Scott & Co., Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (17224-672-30)", "package_ndc": "17224-672-30", "marketing_start_date": "20100101"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (17224-672-60)", "package_ndc": "17224-672-60", "marketing_start_date": "20100101"}], "brand_name": "benzphetamine hydrochloride", "product_id": "17224-672_f5ee265f-9765-de77-e053-2a95a90ac76f", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "17224-672", "dea_schedule": "CIII", "generic_name": "BENZPHETAMINE HYDROCHLORIDE", "labeler_name": "Calvin Scott & Co., 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": "20100101", "listing_expiration_date": "20261231"}