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
7133502911
60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-1)
ndc11
7133502912
30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-2)
ndc11
7133502913
90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-3)
ndc11
7133502914
56 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-4)
ndc11
7133502915
28 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-5)
ndc11
7133502916
10 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-6)
ndc11
7133502917
120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-7)
ndc11
7133502918
180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-8)
ndc11
7133502919
3 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-9)

Annotations

UNII (FDA Substance ID)

6871619Q5X

PANTOPRAZOLE SODIUM

RxCUI 236632

Orange Book

A205119

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": "71335-0291_74c908a1-9dbb-430f-adab-49d147c49e19",
  "productndc": "71335-0291",
  "dosage_form": "TABLET, DELAYED RELEASE",
  "orange_book": {
    "appl_no": "205119",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "001",
        "approval_date": "Jan 26, 2016"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 40MG BASE",
        "product_no": "002",
        "approval_date": "Jan 26, 2016"
      }
    ],
    "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": "ANDA205119",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Pantoprazole",
  "start_marketing_date": "20160620",
  "active_numerator_strength": "20"
}

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