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United States · US · US:68462-209_66bb1c8f-1f66-4834-86a3-a387d076aa22

Moexipril Hydrochloride

Orange BookUNIISPLATC C09AA13

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

Identification

ManufacturerGlenmark Pharmaceuticals Inc., USA
CountryUS (United States)
ATC codeC09AA13
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    6846220901
    100 TABLET, FILM COATED in 1 BOTTLE (68462-209-01)
  • ndc11
    6846220910
    1000 TABLET, FILM COATED in 1 BOTTLE (68462-209-10)
  • ndc11
    6846220990
    90 TABLET, FILM COATED in 1 BOTTLE (68462-209-90)

Annotations

UNII (FDA Substance ID)
Q1UMG3UH45
MOEXIPRIL HYDROCHLORIDE
RxCUI 236066
Orange Book
A090416
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "Q1UMG3UH45",
    "rxcui": "236066",
    "inchikey": "JXRAXHBVZQZSIC-JKVLGAQCSA-N",
    "display_name": "MOEXIPRIL HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "baac91ad-f8ee-4694-89f8-5c47a8eda39a": {
      "match": "brand_token",
      "title": "MOEXIPRIL HYDROCHLORIDE TABLET, FILM COATED [GLENMARK PHARMACEUTICALS INC., USA]",
      "spl_version": "12",
      "published_date": "2026-01-26"
    }
  },
  "productid": "68462-209_66bb1c8f-1f66-4834-86a3-a387d076aa22",
  "productndc": "68462-209",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "090416",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "7.5MG",
        "product_no": "001",
        "approval_date": "Mar 30, 2010"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "15MG",
        "product_no": "002",
        "approval_date": "Mar 30, 2010"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "MOEXIPRIL HYDROCHLORIDE",
  "proprietary_name": "Moexipril Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA090416",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Moexipril Hydrochloride",
  "start_marketing_date": "20101231",
  "active_numerator_strength": "7.5"
}

Related drugs

Other records sharing ATC code C09AA13.

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