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United States · US · US:68071-3400_2d54077e-4c8e-aaae-e063-6394a90adb41

DIETHYLPROPION HYDROCHLORIDE

Orange BookUNIISPLATC A08AA03

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

Identification

ManufacturerNuCare Pharmaceuticals,Inc.
CountryUS (United States)
ATC codeA08AA03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 7

  • ndc11
    6807134000
    112 TABLET in 1 BOTTLE (68071-3400-0)
  • ndc11
    6807134001
    21 TABLET in 1 BOTTLE (68071-3400-1)
  • ndc11
    6807134002
    42 TABLET in 1 BOTTLE (68071-3400-2)
  • ndc11
    6807134003
    30 TABLET in 1 BOTTLE (68071-3400-3)
  • ndc11
    6807134004
    84 TABLET in 1 BOTTLE (68071-3400-4)
  • ndc11
    6807134005
    56 TABLET in 1 BOTTLE (68071-3400-5)
  • ndc11
    6807134007
    14 TABLET in 1 BOTTLE (68071-3400-7)

Annotations

UNII (FDA Substance ID)
19V2PL39NG
DIETHYLPROPION HYDROCHLORIDE
RxCUI 81998
Orange Book
A201212
AA
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "19V2PL39NG",
    "rxcui": "81998",
    "inchikey": "ICFXZZFWRWNZMA-UHFFFAOYSA-N",
    "display_name": "DIETHYLPROPION HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "04f1a804-00f1-48f5-acfa-0ed1a8544784": {
      "match": "brand_token",
      "title": "DIETHYLPROPION HYDROCHLORIDE ER (DIETHYLPROPION HYDROCHLORIDE) TABLET, EXTENDED RELEASE [A-S MEDICATION SOLUTIONS]",
      "spl_version": "29",
      "published_date": "2026-06-01"
    }
  },
  "productid": "68071-3400_2d54077e-4c8e-aaae-e063-6394a90adb41",
  "productndc": "68071-3400",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "201212",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AA",
        "strength": "25MG",
        "product_no": "001",
        "approval_date": "Dec 22, 2010"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": "CIV",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "DIETHYLPROPION HYDROCHLORIDE",
  "proprietary_name": "DIETHYLPROPION HYDROCHLORIDE",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA201212",
  "marketing_category": "ANDA",
  "nonproprietary_name": "DIETHYLPROPION HYDROCHLORIDE",
  "start_marketing_date": "20101227",
  "active_numerator_strength": "25"
}

Related drugs

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