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United States · US · US:51672-4012_34699b9e-d070-64b2-e063-6294a90a0f6d

CLOMIPRAMINE HYDROCHLORIDE

Orange BookUNIISPLATC N06AA04

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

Identification

ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC codeN06AA04
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    5167240124
    60 CAPSULE in 1 BOTTLE (51672-4012-4)
  • ndc11
    5167240125
    90 CAPSULE in 1 BOTTLE (51672-4012-5)
  • ndc11
    5167240121
    100 CAPSULE in 1 BOTTLE (51672-4012-1)
  • ndc11
    5167240126
    30 CAPSULE in 1 BOTTLE (51672-4012-6)

Annotations

UNII (FDA Substance ID)
2LXW0L6GWJ
CLOMIPRAMINE HYDROCHLORIDE
RxCUI 81984
Orange Book
A074694
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "2LXW0L6GWJ",
    "rxcui": "81984",
    "inchikey": "WIMWMKZEIBHDTH-UHFFFAOYSA-N",
    "display_name": "CLOMIPRAMINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "c33d02b1-9a00-4b4a-8f8e-d2679c3838bc": {
      "match": "brand_token",
      "title": "CLOMIPRAMINE HCL POWDER [AX PHARMACEUTICAL CORP]",
      "spl_version": "1",
      "published_date": "2026-04-14"
    }
  },
  "productid": "51672-4012_34699b9e-d070-64b2-e063-6294a90a0f6d",
  "productndc": "51672-4012",
  "dosage_form": "CAPSULE",
  "orange_book": {
    "appl_no": "074694",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "25MG",
        "product_no": "001",
        "approval_date": "Dec 31, 1996"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "002",
        "approval_date": "Dec 31, 1996"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "75MG",
        "product_no": "003",
        "approval_date": "Dec 31, 1996"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CLOMIPRAMINE HYDROCHLORIDE",
  "proprietary_name": "CLOMIPRAMINE HYDROCHLORIDE",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA074694",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Clomipramine Hydrochloride",
  "start_marketing_date": "19961231",
  "active_numerator_strength": "50"
}

Related drugs

Other records sharing ATC code N06AA04.

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