NDC 51672-4111-01 - Phenytoin Sodium
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
- 51672-4111
- Requested NDC
- 51672-4111-01
- Package NDCs from labels
- 51672-4111-6, 51672-4111-1, 51672-4111-3, 51672-4111-0, 51672-4111-01
- Manufacturer
- Major Pharmaceuticals
- Effective date
- 2026-08-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Phenytoin Sodium - Major Pharmaceuticals | Major Pharmaceuticals | 2026-08-20 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenytoin Sodium - A-S Medication Solutions | A-S Medication Solutions | 2026-07-24 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenytoin Sodium - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-05-19 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenytoin Sodium - Coupler LLC | Coupler LLC | 2026-05-13 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenytoin Sodium - Golden State Medical Supply, Inc. | Golden State Medical Supply, Inc. | 2026-04-21 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenytoin Sodium - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-03-25 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenytoin Sodium - Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd., | Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd., | 2026-03-17 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenytoin Sodium - AvPAK | AvPAK | 2026-03-03 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenytoin Sodium - Proficient Rx LP | Proficient Rx LP | 2026-02-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenytoin Sodium - Aphena Pharma Solutions - Tennessee, LLC | Aphena Pharma Solutions - Tennessee, LLC | 2024-12-20 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenytoin Sodium - NCS HealthCare of KY, LLC dba Vangard Labs | NCS HealthCare of KY, LLC dba Vangard Labs | 2023-03-23 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenytoin Sodium - RPK Pharmaceuticals, Inc. | RPK Pharmaceuticals, Inc. | 2020-12-25 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenytoin Sodium - Clinical Solutions Wholesale, LLC | Clinical Solutions Wholesale, LLC | 2020-09-25 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenytoin Sodium - A-S Medication Solutions | A-S Medication Solutions | 2018-07-06 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenytoin Sodium - TYA Pharmaceuticals | TYA Pharmaceuticals | 2014-06-17 | HUMAN PRESCRIPTION DRUG LABEL |
| Extended Phenytoin Sodium Capsules USP, 100 mg | Physicians Total Care, Inc. | 2012-02-12 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenytoin Sodium - Rebel Distributors Corp | Rebel Distributors Corp | 2011-01-04 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenytoin Sodium - Contract Pharmacy Services-PA | Contract Pharmacy Services-PA | 2010-04-06 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-4111-0 | Phenytoin Sodium | 10 in 1 CARTON | CAPSULE, EXTENDED RELEASE | 10 | 16 | |
| 51672-4111-0 | Phenytoin Sodium | 10 in 1 BLISTER PACK | CAPSULE, EXTENDED RELEASE | 10 | 16 | |
| 51672-4111-1 | Phenytoin Sodium | 100 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 100 | 16 | |
| 51672-4111-3 | Phenytoin Sodium | 1000 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 1000 | 16 | |
| 51672-4111-6 | Phenytoin Sodium | 30 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 30 | 16 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-4111 | PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.] | 15 | Current NDC, Legacy NDC, 5 package rows | 20240929_601f7353-225d-4a5d-9810-3869c2c21874.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-4111-1 | EA - Each | 51672-4111 | 0f23fecb-57c3-4685-be86-4d4a9d0bae2b | 1 | 2012-07-24 |
| 51672-4111-3 | EA - Each | 51672-4111 | ce9b3ded-f89d-4b8d-8d40-286c6ac91bdb | 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 |
|---|---|---|---|---|---|---|
| Mineral Primer tinted SPF40 | TITANIUM DIOXIDE, ZINC OXIDE | Oracle Esthetics, LLC | 3542d8d3-35a3-7d63-e063-6394a90a6fd1 | 2025-12-15 | 15FIX9V2JP | |
| Mineral Primer non-tinted SPF40 | TITANIUM DIOXIDE, ZINC OXIDE | Oracle Esthetics, LLC | 354357de-1a85-3bdb-e063-6294a90aa9a2 | 2025-12-15 | 15FIX9V2JP | |
| Mineral Primer tinted SPF40 | TITANIUM DIOXIDE, ZINC OXIDE | Oracle Esthetics, LLC | 35433254-1dc8-a8f3-e063-6394a90a29f0 | 2025-12-15 | 15FIX9V2JP | |
| Complexion Correction Primer Sunscreen clear | TITANIUM DIOXIDE, ZINC OXIDE | MCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY | 357eee3c-1c21-5efb-e063-6294a90a4bb7 | 2025-12-15 | 15FIX9V2JP | |
| Complexion Correction Tinted Primer Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | MCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY | 357e75ec-473e-df76-e063-6294a90a70c7 | 2025-12-15 | 15FIX9V2JP | |
| Complexion Correction Tinted Primer Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | MCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY | 357f2f62-904a-2234-e063-6394a90aee72 | 2025-12-15 | 15FIX9V2JP | |
| Complexion Correction Primer Sunscreen clear | TITANIUM DIOXIDE, ZINC OXIDE | MCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY | 357ff025-84ad-6d77-e063-6394a90aad95 | 2025-12-15 | 15FIX9V2JP | |
| Complexion Correction Tinted Primer Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | MCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY | 358021a2-235b-825b-e063-6394a90a76f5 | 2025-12-15 | 15FIX9V2JP | |
| Tinted Physical Defense | TITANIUM DIOXIDE, ZINC OXIDE | ATLANTA DERMOTOLOGY VEIN & RESEARCH CENTER | 35477ed2-0875-58d5-e063-6294a90a3d5d | 2025-12-15 | 15FIX9V2JP | |
| Tinted Facial Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | HELTON SKIN & LASER INSTITUTE | 35a97770-2db9-99aa-e063-6294a90a459a | 2025-12-15 | 15FIX9V2JP | |
| Non-Tinted Sports Stick | TITANIUM DIOXIDE, ZINC OXIDE | HELTON SKIN & LASER INSTITUTE | 35aa833a-19a1-99e9-e063-6394a90a840f | 2025-12-15 | 15FIX9V2JP | |
| Tinted Facial Primer | TITANIUM DIOXIDE, ZINC OXIDE | BEE NATURALS | 36c3352e-fa51-19ad-e063-6394a90a591b | 2025-12-15 | 15FIX9V2JP | |
| Velvet Tinted Moisturizing Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | SKIN BOSS L.L.C. | 35a871dc-a707-9963-e063-6294a90a4396 | 2025-12-15 | 15FIX9V2JP | |
| Velvet NT Moisturizing Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | SKIN BOSS L.L.C. | 35a8508d-7069-c2d6-e063-6394a90a6219 | 2025-12-15 | 15FIX9V2JP | |
| Proper Protection Plus Primer NT | TITANIUM DIOXIDE, ZINC OXIDE | Skin & Proper LLC | 3596fe93-836b-4f8e-e063-6294a90a674a | 2025-12-15 | 15FIX9V2JP | |
| Proper Protection Plus Primer Tinted | TITANIUM DIOXIDE, ZINC OXIDE | Skin & Proper LLC | 359723bb-6152-9566-e063-6294a90a59e0 | 2025-12-15 | 15FIX9V2JP | |
| Proper Protection Plus Primer NT | TITANIUM DIOXIDE, ZINC OXIDE | Skin & Proper LLC | 3596cd73-0811-32bc-e063-6394a90ad132 | 2025-12-15 | 15FIX9V2JP | |
| Proper Protection Plus Primer Tinted | TITANIUM DIOXIDE, ZINC OXIDE | Skin & Proper LLC | 359782d7-6601-7d96-e063-6394a90af9dc | 2025-12-15 | 15FIX9V2JP | |
| Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | ESTHETICS BY RIKI LLC | 37f1b692-0b80-0536-e063-6294a90ae863 | 2025-12-15 | 15FIX9V2JP | |
| Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | ESTHETICS BY RIKI LLC | 387d5194-bc12-68c1-e063-6394a90ab152 | 2025-12-15 | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.