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United States · US · US:72162-1739_c3daa4ef-b136-479f-b7f7-48ef98c763d5

Lovastatin

Orange BookUNIISPLATC C10AA02

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeC10AA02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 7

  • ndc11
    7216217390
    1000 TABLET in 1 BOTTLE (72162-1739-0)
  • ndc11
    7216217392
    100 TABLET in 1 BOTTLE (72162-1739-2)
  • ndc11
    7216217394
    300 TABLET in 1 BOTTLE (72162-1739-4)
  • ndc11
    7216217395
    500 TABLET in 1 BOTTLE (72162-1739-5)
  • ndc11
    7216217396
    60 TABLET in 1 BOTTLE (72162-1739-6)
  • ndc11
    7216217397
    120 TABLET in 1 BOTTLE (72162-1739-7)
  • ndc11
    7216217399
    90 TABLET in 1 BOTTLE (72162-1739-9)

Annotations

UNII (FDA Substance ID)
9LHU78OQFD
LOVASTATIN
RxCUI 6472
Orange Book
A075991
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "9LHU78OQFD",
    "rxcui": "6472",
    "inchikey": "PCZOHLXUXFIOCF-BXMDZJJMSA-N",
    "display_name": "LOVASTATIN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "f5f265a6-2aa5-4205-9159-40133ae93ac0": {
      "match": "brand_token",
      "title": "LOVASTATIN TABLET [BRYANT RANCH PREPACK]",
      "spl_version": "8",
      "published_date": "2026-06-01"
    }
  },
  "productid": "72162-1739_c3daa4ef-b136-479f-b7f7-48ef98c763d5",
  "productndc": "72162-1739",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "075991",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Jun 5, 2002"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "002",
        "approval_date": "Jun 5, 2002"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "003",
        "approval_date": "Jun 5, 2002"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LOVASTATIN",
  "proprietary_name": "Lovastatin",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA075991",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Lovastatin",
  "start_marketing_date": "20021125",
  "active_numerator_strength": "10"
}

Related drugs

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