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 |
|---|---|---|---|---|---|---|
| Tinted Sunscreen Broad SPF30 | TINTED SUNSCREEN BROAD SPF30 | DOSCHER FAMILY HEALTH NP P.C. | 4d4021ba-4b29-6b81-e063-6294a90a5ea7 | 2026-03-17 | Warnings | 15FIX9V2JP |
| Phenytoin Sodium | PHENYTOIN SODIUM | Sun Pharmaceutical Industries, Inc. | 601f7353-225d-4a5d-9810-3869c2c21874 | 2026-03-17 | Warnings, Adverse reactions | ANDA040684 51672-4111-1 51672-4111-0 51672-4111-6 51672-4111-3 51672-4111 51672411101 855671 4d4421be-75f8-2639-e063-6294a90accd5 601f7353-225d-4a5d-9810-3869c2c21874 4182431BJH |
| HYDRATING TINTED MOISTURIZER SPF50 | HYDRATING TINTED MOISTURIZER SPF50 | NING PTE. LTD. | 4cf8d3d3-eebf-2da0-e063-6294a90a7065 | 2026-03-14 | Warnings | 15FIX9V2JP |
| Drop20 | FUCUS VESICULOSUS, CHELIDONIUM MAJUS, KALI PHOSPHORICUM, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, QUERCUS GLANDIUM SPIRITUS, QUERCUS ROBUR, NUX VOMICA, PHYTOLACCA DECANDRA, ORNITHOGALUM UMBELLATUM, AGNUS CASTUS, BERBERIS AQUIFOLIUM, BERBERIS VULGARIS, SACCHARUM OFFICINALE, SOLIDAGO VIRGAUREA, CALCAREA CARBONICA, CARBO VEGETABILIS, MAGNESIA PHOSPHORICA, NATRUM PHOSPHORICUM, SINAPIS ARVENSIS, FLOS, UBIDECARENONUM, GRAPHITES, HYPOPHYSIS SUIS, PLACENTA TOTALIS SUIS, HYPOTHALAMUS (BOVINE) | Pick Enterprises Corp | baa96813-dc95-472e-a834-880a0cd484a7 | 2026-03-13 | Warnings | C151H8M554 |
| TINTED WATERY SUNSCREEN | TITANIUM DIOXIDE, ZINC OXIDE | KSISTERS PTE. LTD. | 4ced53d0-8bfc-ff8e-e063-6294a90a9dbd | 2026-03-13 | Warnings | 15FIX9V2JP |
| Daily Moisturizing Mineral Sunscreen | BROAD SPECTRUM SPF30 | EDINA PLASTIC SURGERY,LTD. | 4d056e2b-5813-da42-e063-6294a90ac519 | 2026-03-13 | Warnings | 15FIX9V2JP |
| Appetrol 20 | FUCUS VESICULOSUS, CHELIDONIUM MAJUS, KALI PHOSPHORICUM, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, QUERCUS GLANDIUM SPIRITUS, QUERCUS ROBUR, NUX VOMICA, PHYTOLACCA DECANDRA, ORNITHOGALUM UMBELLATUM, AGNUS CASTUS, BERBERIS AQUIFOLIUM, BERBERIS VULGARIS, SACCHARUM OFFICINALE, SOLIDAGO VIRGAUREA, CALCAREA CARBONICA, CARBO VEGETABILIS, MAGNESIA PHOSPHORICA, NATRUM PHOSPHORICUM, SINAPIS ARVENSIS, FLOS, UBIDECARENONUM, GRAPHITES, HYPOPHYSIS SUIS, PLACENTA TOTALIS SUIS, HYPOTHALAMUS (BOVINE) | Carbalor LLC | d66234a3-2477-42be-8f7b-283e3a5f87ed | 2026-03-12 | Warnings | C151H8M554 |
| Neutrogena Healthy Skin Liquid Makeup Broad Spectrum SPF 20 - Cool Bronze 440C | TITANIUM DIOXIDE | Kenvue Brands LLC | 4c335d9c-40ca-c0ce-e063-6394a90ac20a | 2026-03-11 | Warnings | 15FIX9V2JP |
| Artificial Tears | GLYCERIN | Preferred Pharmaceuticals Inc. | dd646c72-8f47-43c6-a734-db0dcc8cd4d1 | 2026-03-06 | Warnings | 3NXW29V3WO |
| cle de peau BEAUTE RADIANT FLUID FOUNDATION NATURAL B50 | OCTINOXATE AND TITANIUM DIOXIDE | SHISEIDO AMERICAS CORPORATION | 4490f968-46b6-44d2-af2d-5130b52c8861 | 2026-03-05 | Warnings | 15FIX9V2JP |
| Walgreens Unscented Pain Relieving | LIDOCAINE HYDROCHLORIDE, BENZYL ALCOHOL | Walgreen Co. | 41eadb4f-2ca5-42a1-e063-6294a90ab4e2 | 2026-03-04 | Warnings | LKG8494WBH |
| Phenytoin Sodium | PHENYTOIN SODIUM | AvPAK | 4c2542b8-ac54-e85d-e063-6294a90a759b | 2026-03-03 | Warnings, Adverse reactions | ANDA040684 50268-719-13 50268-719-11 50268-719 855671 4c253166-859e-cff9-e063-6294a90a7bb7 4c2542b8-ac54-e85d-e063-6294a90a759b 4182431BJH |
| PHENYTOIN SODIUM | PHENYTOIN SODIUM | DIRECT RX | df0bf42b-ce9a-42c3-8c24-46f1ea3bd214 | 2026-02-27 | Warnings, Adverse reactions | 855671 4182431BJH |
| TIBENA EVERY DAY REAL SUN BLOCK | TITANIUM DIOXIDE, ZINC OXIDE | KONAD CO LTD | 211c9930-4f91-cf8f-e063-6394a90a97b3 | 2026-02-26 | Warnings | 15FIX9V2JP |
| CLE DE PEAU BEAUTE RADIANT FLUID FOUNDATION MATTE M B10 | TITANIUM DIOXIDE | Shiseido Americas Corporation | 54f8210f-4934-4ada-89c3-aa89e7a09260 | 2026-02-26 | Warnings | 15FIX9V2JP |
| SHISEIDO UV PROTECTIVE COMPACT (REFILL) FAIR IVORY | OCTINOXATE, OCTOCRYLENE, AND TITANIUM DIOXIDE | SHISEIDO AMERICAS CORPORATION | c05cef12-a6a7-4682-9357-6d77f4ca3267 | 2026-02-25 | Warnings | 15FIX9V2JP |
| cle de peau BEAUTE RADIANT FOUNDATION N M I10 | OCTINOXATE AND TITANIUM DIOXIDE | Shiseido Americas Corporation | 3be1fe06-bd3b-4078-bee9-d3caf8d068ff | 2026-02-25 | Warnings | 15FIX9V2JP |
| cle de peau BEAUTE THE FOUNDATION N M O20 | OCTINOXATE AND TITANIUM DIOXIDE | Shiseido Americas Corporation | 9507f6d1-c11c-428d-8d95-b436f27ba26a | 2026-02-24 | Warnings | 15FIX9V2JP |
| Perfect Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | SKIN PERFECT MEDICAL | 4b93538a-3b3e-90f7-e063-6294a90ab898 | 2026-02-24 | Warnings | 15FIX9V2JP |
| ANTI-AGING TINTED SUNSCREEN | TITANIUM DIOXIDE, ZINC OXIDE | LASER GIRL SKINCARE, LLC | 4b93cd22-1289-29bc-e063-6294a90ab781 | 2026-02-24 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.