Pantoprazole Sodium

Orange BookUNIISPLATC A02BC02

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeA02BC02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 8

ndc11
7133511651
60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-1)
ndc11
7133511652
30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-2)
ndc11
7133511653
90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-3)
ndc11
7133511654
56 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-4)
ndc11
7133511655
28 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-5)
ndc11
7133511656
10 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-6)
ndc11
7133511657
120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-7)
ndc11
7133511658
180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-8)

Annotations

UNII (FDA Substance ID)

6871619Q5X

PANTOPRAZOLE SODIUM

RxCUI 236632

Orange Book

A202038

ABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "6871619Q5X",
    "rxcui": "236632",
    "inchikey": "VNKNFEINTHUQGZ-UHFFFAOYSA-N",
    "display_name": "PANTOPRAZOLE SODIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "52bbab54-9f11-77bc-e063-6394a90ab449": {
      "match": "brand_token",
      "title": "PANTOPRAZOLE SODIUM TABLET, DELAYED RELEASE [COUPLER LLC]",
      "spl_version": "1",
      "published_date": "2026-05-28"
    }
  },
  "productid": "71335-1165_aeabd7ab-9ae8-4fbf-af5e-deaf166965b9",
  "productndc": "71335-1165",
  "dosage_form": "TABLET, DELAYED RELEASE",
  "orange_book": {
    "appl_no": "202038",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "001",
        "approval_date": "Sep 28, 2012"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 40MG BASE",
        "product_no": "002",
        "approval_date": "Sep 28, 2012"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "PANTOPRAZOLE SODIUM",
  "proprietary_name": "Pantoprazole Sodium",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA202038",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Pantoprazole Sodium",
  "start_marketing_date": "20120928",
  "active_numerator_strength": "20"
}

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