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 · 9

ndc11
7133515721
60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-1)
ndc11
7133515722
30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-2)
ndc11
7133515723
90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-3)
ndc11
7133515724
56 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-4)
ndc11
7133515725
28 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-5)
ndc11
7133515726
10 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-6)
ndc11
7133515727
120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-7)
ndc11
7133515728
180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-8)
ndc11
7133515729
3 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-9)

Annotations

UNII (FDA Substance ID)

6871619Q5X

PANTOPRAZOLE SODIUM

RxCUI 236632

Orange Book

A202882

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": "71335-1572_79deea3c-88e7-40f8-910f-644c1cf65f05",
  "productndc": "71335-1572",
  "dosage_form": "TABLET, DELAYED RELEASE",
  "orange_book": {
    "appl_no": "202882",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "001",
        "approval_date": "Sep 10, 2014"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 40MG BASE",
        "product_no": "002",
        "approval_date": "Sep 10, 2014"
      }
    ],
    "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": "ANDA202882",
  "marketing_category": "ANDA",
  "nonproprietary_name": "PANTOPRAZOLE",
  "start_marketing_date": "20140910",
  "active_numerator_strength": "20"
}

Related drugs

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