NDC 66689-036-01 - Phenytoin
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
- 66689-036
- Requested NDC
- 66689-036-01
- Package NDCs from labels
- 66689-036-01, 66689-036-50
- Manufacturer
- VistaPharm, LLC
- Effective date
- 2024-05-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Phenytoin - VistaPharm, LLC | VistaPharm, LLC | 2024-05-09 | 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 |
|---|---|---|---|---|---|
| 66689-036-50 | 2024-01-30 | C162847 | 48780-1 | 1030e364-fcc6-111a-e063-dadaa90a10e2 | These highlights do not include all the information needed to use PHENYTOIN ORAL SUSPENSION safely and effectively. See full prescribing information for PHENYTOIN ORAL SUSPENSION. PHENYTOIN oral suspension Initial U.S. Approval: 1953 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 66689-036-01 | ML - Milliliter | 66689-036 | 55e6e511-b376-4b6d-9876-c161285ad4c2 | 1 | 2012-07-24 |
| 66689-036-50 | ML - Milliliter | 66689-036 | 099bc12b-07cc-470d-8e68-2718eb515a9d | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Phenytoin | ACTIVE INGREDIENT | 6158TKW0C5 | PHENYTOIN SUSPENSION [VISTAPHARM INC.] | 3 | |
| Phenytoin | ACTIVE MOIETY | 6158TKW0C5 | PHENYTOIN SUSPENSION [VISTAPHARM INC.] | 3 | |
| Anhydrous Citric Acid | INACTIVE INGREDIENT | XF417D3PSL | PHENYTOIN SUSPENSION [VISTAPHARM INC.] | 3 | |
| Carboxymethylcellulose Sodium | INACTIVE INGREDIENT | K679OBS311 | PHENYTOIN SUSPENSION [VISTAPHARM INC.] | 3 | |
| FD&C Yellow No. 6 | INACTIVE INGREDIENT | H77VEI93A8 | PHENYTOIN SUSPENSION [VISTAPHARM INC.] | 3 | |
| Glycerin | INACTIVE INGREDIENT | PDC6A3C0OX | PHENYTOIN SUSPENSION [VISTAPHARM INC.] | 3 | |
| Magnesium Aluminum Silicate | INACTIVE INGREDIENT | 6M3P64V0NC | PHENYTOIN SUSPENSION [VISTAPHARM INC.] | 3 | |
| Polysorbate 80 | INACTIVE INGREDIENT | 6OZP39ZG8H | PHENYTOIN SUSPENSION [VISTAPHARM INC.] | 3 | |
| Sodium Benzoate | INACTIVE INGREDIENT | OJ245FE5EU | PHENYTOIN SUSPENSION [VISTAPHARM INC.] | 3 | |
| Sucrose | INACTIVE INGREDIENT | C151H8M554 | PHENYTOIN SUSPENSION [VISTAPHARM INC.] | 3 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | PHENYTOIN SUSPENSION [VISTAPHARM INC.] | 3 |
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 |
|---|---|---|---|---|---|---|
| Fendall 2000 Pure Flow | PURIFIED WATER | Honeywell Safety Products USA, Inc. | 37dead3e-60cb-88ae-e063-6294a90a8f70 | 2026-06-24 | Warnings | 059QF0KO0R |
| Bacteriostatic Water | BACTERIOSTATIC WATER | Fujian Genohope Biotech Ltd. | 54f66b82-c9e5-a2bc-e063-6394a90adbbc | 2026-06-23 | 059QF0KO0R | |
| Rohto Cool Relief | NAPHAZOLINE HYDROCHLORIDE, POLYSORBATE 80 | The Mentholatum Company | dc8f1ff3-87ae-47ca-815f-5a0e34f8cf30 | 2026-06-19 | Warnings | 6OZP39ZG8H |
| Humalog | INSULIN LISPRO | Eli Lilly and Company | c8ecbd7a-0e22-4fc7-a503-faa58c1b6f3f | 2026-06-16 | Warnings, Adverse reactions | 059QF0KO0R |
| Glycerin | GLYCERIN SUPPOSITORY | Everpharm LLC | 546347e5-841e-15ca-e063-6294a90a0c8b | 2026-06-16 | Warnings | PDC6A3C0OX |
| Glycerin | GLYCERIN SUPPOSITORY | Everpharm LLC | 5463f869-2b92-4551-e063-6394a90ad6f9 | 2026-06-16 | Warnings | PDC6A3C0OX |
| MINICA-S | GLYCERIN | Sato Pharmaceutical Co., Ltd. | 687902eb-e702-4e87-a0ce-9add05e3cbc1 | 2026-06-16 | Warnings | PDC6A3C0OX |
| E-Z-GAS II | ANTACID/ANTIFLATULENT | E-Z-EM, INC. | 4e12e1cb-b033-076d-e054-00144ff8d46c | 2026-06-15 | Warnings | XF417D3PSL |
| WALGREEN GLYCERIN ADULT | GLYCERIN SUPPOSITORY | Walgreens | 20c44346-0b29-7364-e063-6294a90a648f | 2026-06-15 | Warnings | PDC6A3C0OX |
| WALGREENS GLYCERIN | GLYCERIN SUSPENSION | Walgreens | 20c44346-0b2b-7364-e063-6294a90a648f | 2026-06-15 | Warnings | PDC6A3C0OX |
| Lubricant Eye | CARBOXYMETHYLCELLULOSE SODIUM 0.5% | CARDINAL HEALTH 110, LLC. DBA LEADER | 51a2d74f-5ff3-9921-e063-6294a90a345a | 2026-06-15 | Warnings | K679OBS311 |
| Lubricant Eye | CARBOXYMETHYLCELLULOSE SODIUM | Rugby Laboratories | 51cadca6-a31b-c1b5-e063-6394a90a34d3 | 2026-06-15 | Warnings | K679OBS311 |
| BM BM70 DROPS | ANTIM CURD, FERR MET, PHOSPHORUS, SULPHUR, WIESBADEN, THUJA, VERATRUM ALB | Total Operations Management LLC DBA:Bestmade Natural Products Micro | 54113d1f-e8e7-6b4c-e063-6394a90a0edf | 2026-06-12 | Warnings | 059QF0KO0R |
| Sodium Citrate and Citric Acid | SODIUM CITRATE AND CITRIC ACID MONOHYDRATE | Cardinal Health 107, LLC | b3d5225c-0ee4-481e-b9ec-bc5e1321096d | 2026-06-12 | Adverse reactions | XF417D3PSL |
| BM BM70 DROPS | ANTIM CURD, FERR MET, PHOSPHORUS, SULPHUR, WIESBADEN, THUJA, VERATRUM ALB | BM Private Limited | 53fa21d9-1f80-2e69-e063-6394a90ab9f3 | 2026-06-11 | Warnings | 059QF0KO0R |
| Equaline Hemorrhoidal | GLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUM | United Natural Foods, Inc. dba UNFI | bf87824a-522d-46da-81b6-e30ea11a2235 | 2026-06-11 | Warnings | PDC6A3C0OX |
| XIMONTH Fungi Free Bee Venom Nail Soothing Serum | GLYCERIN | Shantou Ximonth Biotechnology Co., Ltd. | 53bab969-8407-6334-e063-6294a90aa5d1 | 2026-06-08 | Warnings | 059QF0KO0R |
| Chloraseptic Sore Throat Max | PHENOL AND GLYCERIN | Prestige Brands Holdings, Inc. | 882c940c-b3c3-4aa4-8d64-e4260f066ff4 | 2026-06-08 | Warnings | PDC6A3C0OX |
| REFRESH CELLUVISC | CARBOXYMETHYLCELLULOSE SODIUM | Allergan, Inc. | b32ed9e8-d091-4f16-b416-5a62cdfee49a | 2026-06-05 | Warnings | K679OBS311 |
| Hemorrhoidal | GLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUM | HyVee Inc | b867f691-7a13-4659-b664-06aa36899310 | 2026-06-03 | Warnings | PDC6A3C0OX |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.