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
7133514291
90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-1)
ndc11
7133514292
30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-2)
ndc11
7133514293
60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-3)
ndc11
7133514294
58 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-4)
ndc11
7133514295
14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-5)
ndc11
7133514296
100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-6)
ndc11
7133514297
10 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-7)
ndc11
7133514298
120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-8)
ndc11
7133514299
180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1429-9)

Annotations

UNII (FDA Substance ID)

6871619Q5X

PANTOPRAZOLE SODIUM

RxCUI 236632

Orange Book

A090970

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": "71335-1429_5f80809c-74f4-49e3-863e-d9c1244ba956",
  "productndc": "71335-1429",
  "dosage_form": "TABLET, DELAYED RELEASE",
  "orange_book": {
    "appl_no": "090970",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "001",
        "approval_date": "Jan 19, 2011"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 40MG BASE",
        "product_no": "002",
        "approval_date": "Jan 19, 2011"
      }
    ],
    "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": "ANDA090970",
  "marketing_category": "ANDA",
  "nonproprietary_name": "pantoprazole sodium",
  "start_marketing_date": "20110119",
  "active_numerator_strength": "40"
}

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