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United States · US · US:71335-0451_98aa03d7-8df0-4b01-8371-9761a0176afa

BENZPHETAMINE HYDROCHLORIDE

Orange BookUNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 9

  • ndc11
    7133504511
    30 TABLET in 1 BOTTLE (71335-0451-1)
  • ndc11
    7133504512
    7 TABLET in 1 BOTTLE (71335-0451-2)
  • ndc11
    7133504513
    14 TABLET in 1 BOTTLE (71335-0451-3)
  • ndc11
    7133504514
    21 TABLET in 1 BOTTLE (71335-0451-4)
  • ndc11
    7133504515
    42 TABLET in 1 BOTTLE (71335-0451-5)
  • ndc11
    7133504516
    84 TABLET in 1 BOTTLE (71335-0451-6)
  • ndc11
    7133504517
    60 TABLET in 1 BOTTLE (71335-0451-7)
  • ndc11
    7133504518
    90 TABLET in 1 BOTTLE (71335-0451-8)
  • ndc11
    7133504519
    120 TABLET in 1 BOTTLE (71335-0451-9)

Annotations

UNII (FDA Substance ID)
43DWT87QT7
BENZPHETAMINE HYDROCHLORIDE
RxCUI 142425
Orange Book
A090968
AA
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "43DWT87QT7",
    "rxcui": "142425",
    "inchikey": "ANFSNXAXVLRZCG-RSAXXLAASA-N",
    "display_name": "BENZPHETAMINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "2b7014af-0cc9-4199-90f2-ec07ac02f8cf": {
      "match": "brand_token",
      "title": "BENZPHETAMINE HYDROCHLORIDE TABLET [PD-RX PHARMACEUTICALS, INC.]",
      "spl_version": "25",
      "published_date": "2025-11-17"
    }
  },
  "productid": "71335-0451_98aa03d7-8df0-4b01-8371-9761a0176afa",
  "productndc": "71335-0451",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "090968",
    "products": [
      {
        "rs": true,
        "rld": false,
        "te_code": "AA",
        "strength": "50MG",
        "product_no": "001",
        "approval_date": "Jul 20, 2010"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": "CIII",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "BENZPHETAMINE HYDROCHLORIDE",
  "proprietary_name": "BENZPHETAMINE HYDROCHLORIDE",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA090968",
  "marketing_category": "ANDA",
  "nonproprietary_name": "benzphetamine hydrochloride",
  "start_marketing_date": "20100721",
  "active_numerator_strength": "50"
}

Access this data programmatically

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