benzphetamine hydrochloride

Generic: benzphetamine hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benzphetamine hydrochloride
Generic Name benzphetamine hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

benzphetamine hydrochloride 50 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-541
Product ID 43063-541_41393fbe-29e5-dd10-e063-6394a90a5a13
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 43063541
Hyphenated Format 43063-541

Supplemental Identifiers

RxCUI
904368
UPC
0343063541609
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
  • 14 TABLET in 1 BOTTLE, PLASTIC (43063-541-14)
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-541-30)
  • 45 TABLET in 1 BOTTLE, PLASTIC (43063-541-45)
  • 60 TABLET in 1 BOTTLE, PLASTIC (43063-541-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (43063-541-90)
  • 120 TABLET in 1 BOTTLE, PLASTIC (43063-541-98)
source: ndc

Packages (6)

43063-541-14 14 TABLET in 1 BOTTLE, PLASTIC (43063-541-14) 43063-541-30 30 TABLET in 1 BOTTLE, PLASTIC (43063-541-30) 43063-541-45 45 TABLET in 1 BOTTLE, PLASTIC (43063-541-45) 43063-541-60 60 TABLET in 1 BOTTLE, PLASTIC (43063-541-60) 43063-541-90 90 TABLET in 1 BOTTLE, PLASTIC (43063-541-90) 43063-541-98 120 TABLET in 1 BOTTLE, PLASTIC (43063-541-98)

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": "41393fbe-29e5-dd10-e063-6394a90a5a13", "openfda": {"upc": ["0343063541609"], "unii": ["43DWT87QT7"], "rxcui": ["904368"], "spl_set_id": ["2b7014af-0cc9-4199-90f2-ec07ac02f8cf"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (43063-541-14)", "package_ndc": "43063-541-14", "marketing_start_date": "20141022"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-541-30)", "package_ndc": "43063-541-30", "marketing_start_date": "20141022"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE, PLASTIC (43063-541-45)", "package_ndc": "43063-541-45", "marketing_start_date": "20141022"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-541-60)", "package_ndc": "43063-541-60", "marketing_start_date": "20141022"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-541-90)", "package_ndc": "43063-541-90", "marketing_start_date": "20141022"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE, PLASTIC (43063-541-98)", "package_ndc": "43063-541-98", "marketing_start_date": "20100721"}], "brand_name": "BENZPHETAMINE HYDROCHLORIDE", "product_id": "43063-541_41393fbe-29e5-dd10-e063-6394a90a5a13", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "43063-541", "dea_schedule": "CIII", "generic_name": "benzphetamine hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, 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"}