BENZPHETAMINE HYDROCHLORIDE

Orange BookUNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerKVK-TECH, INC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
1070204001
100 TABLET in 1 BOTTLE (10702-040-01)
ndc11
1070204003
30 TABLET in 1 BOTTLE (10702-040-03)
ndc11
1070204010
1000 TABLET in 1 BOTTLE (10702-040-10)
ndc11
1070204050
500 TABLET in 1 BOTTLE (10702-040-50)

Annotations

UNII (FDA Substance ID)

43DWT87QT7

BENZPHETAMINE HYDROCHLORIDE

RxCUI 142425

Orange Book

A090968

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": "10702-040_15d75638-8ac7-e610-e063-6394a90af99c",
  "productndc": "10702-040",
  "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"
}

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