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United States · US · US:71335-0807_e6e99a77-7dd9-4fd5-a91a-cb09a573bd58

Esomeprazole Magnesium

Orange BookUNIISPLATC A02BC05

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeA02BC05
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 8

  • ndc11
    7133508071
    30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0807-1)
  • ndc11
    7133508072
    10 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0807-2)
  • ndc11
    7133508073
    60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0807-3)
  • ndc11
    7133508074
    90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0807-4)
  • ndc11
    7133508075
    42 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0807-5)
  • ndc11
    7133508076
    120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0807-6)
  • ndc11
    7133508077
    180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0807-7)
  • ndc11
    7133508078
    20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0807-8)

Annotations

UNII (FDA Substance ID)
36H71644EQ
ESOMEPRAZOLE MAGNESIUM DIHYDRATE
RxCUI 1601995
Orange Book
A205606
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "36H71644EQ",
    "rxcui": "1601995",
    "inchikey": "DBOUSUONOXEWHU-VCKZSRROSA-N",
    "display_name": "ESOMEPRAZOLE MAGNESIUM DIHYDRATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "6a21f085-b60b-49b7-8098-99ccdc43dde3": {
      "match": "brand_token",
      "title": "ESOMEPRAZOLE MAGNESIUM DELAYED-RELEASE 20 MG (OTC) CAPSULE, DELAYED RELEASE ESOMEPRAZOLE MAGNESIUM DELAYED RELEASE 20 MG MINI CAPSULE, DELAYED RELEASE [MARKSANS PHARMA LIMITED]",
      "spl_version": "3",
      "published_date": "2026-06-02"
    }
  },
  "productid": "71335-0807_e6e99a77-7dd9-4fd5-a91a-cb09a573bd58",
  "productndc": "71335-0807",
  "dosage_form": "CAPSULE, DELAYED RELEASE",
  "orange_book": {
    "appl_no": "205606",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "001",
        "approval_date": "Apr 21, 2016"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 40MG BASE",
        "product_no": "002",
        "approval_date": "Apr 21, 2016"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ESOMEPRAZOLE MAGNESIUM DIHYDRATE",
  "proprietary_name": "Esomeprazole Magnesium",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA205606",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Esomeprazole Magnesium",
  "start_marketing_date": "20160421",
  "active_numerator_strength": "20"
}

Related drugs

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