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 |
|---|---|---|---|---|---|---|
| Replenishing Tinted Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | Beauty Journey Studio LLC | 3738a0c3-5c07-e49b-e063-6394a90a38e9 | 2025-12-09 | 15FIX9V2JP | |
| Replenishing Non Tinted Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | Beauty Journey Studio LLC | 37385fc6-1cde-8aa6-e063-6294a90a6017 | 2025-12-09 | 15FIX9V2JP | |
| Skin Filter Matte SPF | TITANIUM DIOXIDE, ZINC OXIDE | MALORIE MILES | 3647f983-9e75-8955-e063-6294a90af162 | 2025-12-08 | 15FIX9V2JP | |
| Skin Filter Matte SPF | TITANIUM DIOXIDE, ZINC OXIDE | MALORIE MILES | 3649f758-e31b-3c6a-e063-6294a90a5c36 | 2025-12-08 | 15FIX9V2JP | |
| Matte Shield SPF | TITANIUM DIOXIDE, ZINC OXIDE | ACNE SOLUTIONS NYC INC | 3bb582ec-71e7-4ad8-e063-6394a90a94d4 | 2025-12-08 | Warnings | 15FIX9V2JP |
| Mineral Based Sunscreen Stick Non-Tinted | TITANIUM DIOXIDE, ZINC OXIDE | KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION | 3245561d-a90c-7bf0-e063-6394a90ab3b6 | 2025-12-08 | 15FIX9V2JP | |
| Mineral Based Sunscreen Stick Tinted | TITANIUM DIOXIDE, ZINC OXIDE | KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION | 3245c1f7-2c1b-b6ad-e063-6394a90aaee6 | 2025-12-08 | 15FIX9V2JP | |
| Mineral Based Foam Sunscreen Tinted | TITANIUM DIOXIDE, ZINC OXIDE | KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION | 32465271-abb9-d03f-e063-6294a90a990e | 2025-12-08 | 15FIX9V2JP | |
| Mineral Based Foam Sunscreen Non-Tinted | TITANIUM DIOXIDE, ZINC OXIDE | KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION | 32486bfb-0cc8-0283-e063-6394a90a9967 | 2025-12-08 | 15FIX9V2JP | |
| Healthy Mineral Sunscreen No Shine - No Tint | TITANIUM DIOXIDE, ZINC OXIDE | Zen Dermatology, Inc. | 31572a16-5f60-565f-e063-6394a90ab8c9 | 2025-12-08 | Warnings | 15FIX9V2JP |
| AcneFix Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | ACNEFIX INC. | 315894b7-ac1b-0982-e063-6294a90ab879 | 2025-12-08 | 15FIX9V2JP | |
| Shunly Natural Cover SPF50 | TITANIUM DIOXIDE, ZINC OXIDE | Shunly Skin Care | a64e373b-b3f6-4024-b5f5-253783485cd6 | 2025-12-08 | Warnings | 15FIX9V2JP |
| AcneFix Non-Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | ACNEFIX INC. | 31583c7e-365a-d899-e063-6394a90aa63f | 2025-12-08 | 15FIX9V2JP | |
| Mineral Fusion Tinted | TITANIUM DIOXIDE, ZINC OXIDE | FOREFRONT DERMATOLOGY, S.C. | 334ec844-5560-50f7-e063-6394a90a01be | 2025-12-08 | 15FIX9V2JP | |
| Mineral Fusion Tinted | TITANIUM DIOXIDE, ZINC OXIDE | FOREFRONT DERMATOLOGY, S.C. | 334f90d6-68e5-db37-e063-6294a90a5fb1 | 2025-12-08 | 15FIX9V2JP | |
| Silk Screen | TITANIUM DIOXIDE, ZINC OXIDE | Skin Apeel, Inc. | 3c44baf4-9555-faad-e063-6294a90ab24f | 2025-12-08 | Warnings | 15FIX9V2JP |
| Glow Stick | TITANIUM DIOXIDE, ZINC OXIDE | Skin Apeel, Inc. | 3c54b857-c017-a953-e063-6394a90a38df | 2025-12-08 | Warnings | 15FIX9V2JP |
| Lip Shield | TITANIUM DIOXIDE, ZINC OXIDE | Skin Apeel, Inc. | 3c545e55-3f55-842b-e063-6394a90ae48e | 2025-12-08 | Warnings | 15FIX9V2JP |
| Bare Barrier Sport | TITANIUM DIOXIDE, ZINC OXIDE | Skin Apeel, Inc. | 3c580794-eda3-de57-e063-6294a90a0303 | 2025-12-08 | Warnings | 15FIX9V2JP |
| Flawless Brightening Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | Flawless Skin Care LLC | 312e9ca0-a388-a546-e063-6294a90a15d6 | 2025-12-08 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.