DIETHYLPROPION HYDROCHLORIDE

Orange BookUNIISPLATC A08AA03

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeA08AA03

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 10

ndc11
7133517790
42 TABLET in 1 BOTTLE (71335-1779-0)
ndc11
7133517791
28 TABLET in 1 BOTTLE (71335-1779-1)
ndc11
7133517792
90 TABLET in 1 BOTTLE (71335-1779-2)
ndc11
7133517793
30 TABLET in 1 BOTTLE (71335-1779-3)
ndc11
7133517794
14 TABLET in 1 BOTTLE (71335-1779-4)
ndc11
7133517795
21 TABLET in 1 BOTTLE (71335-1779-5)
ndc11
7133517796
7 TABLET in 1 BOTTLE (71335-1779-6)
ndc11
7133517797
60 TABLET in 1 BOTTLE (71335-1779-7)
ndc11
7133517798
84 TABLET in 1 BOTTLE (71335-1779-8)
ndc11
7133517799
56 TABLET in 1 BOTTLE (71335-1779-9)

Annotations

UNII (FDA Substance ID)

19V2PL39NG

DIETHYLPROPION HYDROCHLORIDE

RxCUI 81998

Orange Book

A201212

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": "71335-1779_03ffc9bf-1d54-4e09-9e9c-374a73871e60",
  "productndc": "71335-1779",
  "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"
}

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