NDC 0008-0844-01 - Protonix Delayed-Release
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 0008-0844
- Requested NDC
- 0008-0844-01
- Package NDCs from labels
- 0008-0844-01, 0008-0844-02
- Manufacturer
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | AndersonBrecon Inc. | Takeda GmbH
- Effective date
- 2026-05-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PANTOPRAZOLE - Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | AndersonBrecon Inc. | Takeda GmbH | Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | AndersonBrecon Inc. | Takeda GmbH | 2026-05-18 | HUMAN PRESCRIPTION DRUG LABEL |
| Protonix Delayed-Release - Cardinal Health 107, LLC | Cardinal Health 107, LLC | 2024-10-10 | HUMAN PRESCRIPTION DRUG LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2012-07-24 | Indexing - Billing Unit |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0008-0844-02 | 2024-01-30 | C162847 | 48780-1 | 1030e364-f951-111a-e063-dadaa90a10e2 | These highlights do not include all the information needed to use PROTONIX safely and effectively. See full prescribing information for PROTONIX. PROTONIX (pantoprazole sodium) delayed-release tablets, for oral use PROTONIX (pantoprazole sodium) for delayed-release oral suspension Initial U.S. approval: 2000 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0008-0844-01 | ProtonixDelayed-Release | 1 in 1 PACKET | GRANULE, DELAYED RELEASE | 1 | 48 | |
| 0008-0844-02 | ProtonixDelayed-Release | 30 in 1 CARTON | GRANULE, DELAYED RELEASE | 30 | 48 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 0008-0844 | PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS LLC, A SUBSIDIARY OF PFIZER INC.] | 47 | Current NDC, Legacy NDC, 2 package rows | 20240719_08098cb2-c048-4640-f387-6beec4a38936.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0008-0844-01 | EA - Each | 0008-0844 | a4a64248-a74b-44f3-85c5-bfd22d4cd462 | 1 | 2012-07-24 |
| 0008-0844-02 | EA - Each | 0008-0844 | 923dad3a-0648-4fe5-b4ea-526fe7657d8d | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Neutrogena Collagen Bank SPF Moisturizer Sunscreen Broad Spectrum SPF 30 and Neutrogena Collagen Bank Moisturizer | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | Acupac Packaging, Inc. | 4ef5baf7-00b1-97aa-e063-6294a90aab9c | 2026-04-08 | Warnings | 15FIX9V2JP |
| Neutrogena Mineral Ultra Sheer Face SPF 70 | TITANIUM DIOXIDE, ZINC OXIDE | Acupac Packaging, Inc. | 4ef5dcd4-b2d0-bcd1-e063-6294a90a871f | 2026-04-08 | Warnings | 15FIX9V2JP |
| Neutrogena Mineral Invisible Daily Defense Face Sunscreen Broad Spectrum SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | Acupac Packaging, Inc. | 4ef6b5fb-5495-001c-e063-6394a90ab7b3 | 2026-04-08 | Warnings | 15FIX9V2JP |
| Pantoprazole Sodium | PANTOPRAZOLE SODIUM | Northstar Rx LLC | 7e0c5dac-6832-4692-b012-ca59d5e88987 | 2026-04-08 | Warnings, Adverse reactions | 6871619Q5X |
| Nu Colour Bioadaptive BB Plus Foundation - Light Golden | TITANIUM DIOXIDE | NSE Products, Inc. | faae6f47-19f3-41cb-8e0d-388569b5c73d | 2026-04-07 | Warnings | 15FIX9V2JP |
| Ultra Sunscreen | OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE | Jiangsu Senwo Medical Technology Co., Ltd. | 4ed974b8-6c11-08e0-e063-6294a90a7713 | 2026-04-07 | Warnings | 15FIX9V2JP |
| Neutrogena MINERAL UV TINT FACE MEDIUM DEEP SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | Acupac Packaging, Inc | 4ee39bbf-b7d7-8f87-e063-6294a90a2539 | 2026-04-07 | Warnings | 15FIX9V2JP |
| H-Focus Formula | AGNUS CASTUS, AVENA SATIVA, BARYTA CARBONICA, IGNATIA AMARA, LYCOPODIUM CLAVATUM, NATRUM CARBONICUM, NATRUM MURIATICUM, PHOSPHORICUM ACIDUM, SILICEA, ZINCUM METALLICUM | Healing Natural Oils LLC | 4ee42911-3064-7f55-e063-6294a90abcc7 | 2026-04-07 | Warnings | 45P3261C7T |
| Pantoprazole Sodium | PANTOPRAZOLE SODIUM | Safecor Health LLC | 5e1cbf26-d379-4315-8732-3939968f32c0 | 2026-04-07 | Warnings, Adverse reactions | 314200 6871619Q5X |
| H-Mood Formula | AGRIMONIA EUPATORIA, FLOS, ANACARDIUM ORIENTALE, AURUM METALLICUM, AVENA SATIVA, BORAGO OFFICINALIS, CAPSICUM ANNUUM, CARPINUS BETULUS, FLOS, CIMICIFUGA RACEMOSA, CINCHONA OFFICINALIS, HYPERICUM PERFORATUM, KALI BROMATUM, LARIX DECIDUA, FLOS, NATRUM CARBONICUM, NATRUM MURIATICUM, NATRUM SULPHURICUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, PULSATILLA, SILICEA, SINAPSIS ARVENSIS, FLOS, TABACUM | Healing Natural Oils LLC | 4ee5c82e-9edf-c36e-e063-6394a90a237f | 2026-04-07 | Warnings | 45P3261C7T |
| Nu Colour Bioadaptive BB plus Foundation - Beige | TITANIUM DIOXIDE | NSE Products, Inc. | f74e83fe-41a0-4998-ae53-30ed5af47592 | 2026-04-07 | Warnings | 15FIX9V2JP |
| pantoprazole sodium | PANTOPRAZOLE SODIUM | Granules Pharmaceuticals Inc. | 8f2fb647-15bc-41cb-84a4-02e956e614fc | 2026-04-06 | Warnings, Adverse reactions | 251872 314200 6871619Q5X |
| Protonix I.V. | PANTOPRAZOLE SODIUM | Cardinal Health 107, LLC | 50802e19-72d3-4130-8d14-eb94361b38e7 | 2026-04-06 | Warnings, Adverse reactions | 6871619Q5X |
| EltaMD Skincare UV AOX Elements SPF50 Tinted | TITANIUM DIOXIDE, ZINC OXIDE SUNSCREEN | CP Skin Health Group, Inc | 2c74209d-9b88-4c32-ad42-cd6de16c1fef | 2026-04-03 | Warnings | 15FIX9V2JP |
| EltaMD UV Restore Tinted | TITANIUM DIOXIDE AND ZINC OXIDE SUNSCREEN | CP Skin Health Group, Inc | 4fc18856-01b3-43ed-9e1b-b4394e31aa3c | 2026-04-03 | Warnings | 15FIX9V2JP |
| Sunscreen for baby SPF50plus | OCTOCRYLENE,ETHYLHEXYL METHOXYCINNAMATE,TITANIUM DIOXIDE,ETHYLHEXYL SALICYLATE | Guangzhou Senmai Biotechnology Co., Ltd. | 1cb7fbca-0874-ae53-e063-6294a90ab42a | 2026-04-02 | Warnings | 15FIX9V2JP |
| TiZO3 | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals, LTD | 4e7bdec2-abcc-0267-e063-6394a90ae47a | 2026-04-02 | Warnings | 15FIX9V2JP |
| EltaMD UV Restore | TITANIUM DIOXIDE, ZINC OXIDE SUNSCREEN | CP Skin Health Group, Inc | 17b47994-82d6-4f9d-8249-bdb55106c9b3 | 2026-04-02 | Warnings | 15FIX9V2JP |
| Clinical Skin Filter Tinted Sunscreen | CLINICAL SKIN FILTER TINTED SUNSCREEN | BY KIN AESTHETICS LLC | 4e69a8a3-8dbb-577a-e063-6294a90a6a23 | 2026-04-01 | Warnings | 15FIX9V2JP |
| Krx Aesthetics All Day Glow Sunblocker | KRX AESTHETICS ALL DAY GLOW SUNBLOCKER | BY KIN AESTHETICS LLC | 4e69df43-393b-bc09-e063-6394a90a275a | 2026-04-01 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.