NDC 0641-0367-21 - Dexamethasone Sodium Phosphate
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
- 0641-0367
- Requested NDC
- 0641-0367-21
- Package NDCs from labels
- 0641-0367-21, 0641-0367-25
- Manufacturer
- Cardinal Health 107, LLC
- Effective date
- 2026-04-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dexamethasone Sodium Phosphate - Cardinal Health 107, LLC | Cardinal Health 107, LLC | 2026-04-21 | HUMAN PRESCRIPTION DRUG LABEL |
| Dexamethasone Sodium Phosphate Injection, USP Rx only | REMEDYREPACK INC. | 2026-03-16 | HUMAN PRESCRIPTION DRUG LABEL |
| Dexamethasone Sodium Phosphate - A-S Medication Solutions | A-S Medication Solutions | 2026-02-02 | HUMAN PRESCRIPTION DRUG LABEL |
| Dexamethasone Sodium Phosphate Injection, USP Rx only | Hikma Pharmaceuticals USA Inc. | 2026-01-22 | HUMAN PRESCRIPTION DRUG LABEL |
| DEXAMETHASONE SODIUM PHOSPHATE - HF Acquisition Co LLC, DBA HealthFirst | HF Acquisition Co LLC, DBA HealthFirst | 2024-01-04 | HUMAN PRESCRIPTION DRUG LABEL |
| Dexamethasone Sodium Phosphate - Medical Purchasing Solutions, LLC | Medical Purchasing Solutions, LLC | 2023-05-23 | HUMAN PRESCRIPTION DRUG LABEL |
| ReadySharp Anesthetics plus Dexamethasone - Terrain Pharmaceuticals | Terrain Pharmaceuticals | 2017-12-19 | 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 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0641-0367-21 | Dexamethasone Sodium Phosphate | 1 mL in 1 VIAL | INJECTION | 1 | 21 | |
| 0641-0367-25 | Dexamethasone Sodium Phosphate | 25 in 1 CARTON | INJECTION | 25 | 21 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0641-0367-21 | ML - Milliliter | 0641-0367 | 0ac648a0-35ec-434c-b33d-1645e8a8cc74 | 1 | 2012-07-24 |
| 0641-0367-25 | ML - Milliliter | 0641-0367 | b7f2dd89-0a90-48e6-ad12-aef4345ecf38 | 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 |
|---|---|---|---|---|---|---|
| BeardedMoney | LIDOCAINE HYDROCHLORIDE | Sambria Pharmaceuticals, LLC | 35ff688b-75c5-4780-b294-192af780d705 | 2025-11-12 | Warnings | V13007Z41A |
| NeuroMed 7 Topical Pain Relief | LIDOCAINE HYDROCHLORIDE | Sambria Pharmaceuticals, LLC | f199f56b-d971-4cf8-834d-babb5c2ff81a | 2025-11-12 | Warnings | V13007Z41A |
| NeuroMed Topical Anesthetic 7 | LIDOCAINE HYDROCHLORIDE | Sambria Pharmaceuticals | 8a2b6b76-6bcc-4f52-b037-e6cbc74f8377 | 2025-11-12 | Warnings | V13007Z41A |
| NeuroMed Topical Anesthetic 7 | LIDOCAINE HYDROCHLORIDE | Sambria Pharmaceuticals | 67b25c37-db32-4980-88b0-b07712345939 | 2025-11-12 | Warnings | V13007Z41A |
| Lidozall | LIDOCAINE HYDROCHLORIDE | V2 Pharma LLC | 1eb2dfb2-3ad1-488b-aed9-17220e34a10c | 2025-11-12 | Warnings | V13007Z41A |
| Lidozall Plus | LIDOCAINE HYDROCHLORIDE | V2 Pharma LLC | ba3cbb15-f4ed-443e-af43-a758481acb0b | 2025-11-12 | Warnings | V13007Z41A |
| Eyesaline Eyewash Concentrate | PURIFIED WATER | Honeywell Safety Products USA, Inc. | 3765c251-eb14-d60f-e063-6294a90a6a4d | 2025-11-12 | Warnings | 059QF0KO0R |
| Eyesaline Emergency Eyewash | PURIFIED WATER | Honeywell Safety Products USA, Inc. | 37f244fd-c02f-e66a-e063-6394a90aed81 | 2025-11-12 | Warnings | 059QF0KO0R |
| Dexamethasone Sodium Phosphate | DEXAMETHASONE SODIUM PHOSPHATE | Eugia US LLC | 29947f67-7868-40af-8ad2-a61f7149b44c | 2025-11-12 | Warnings, Adverse reactions | 1812079 AI9376Y64P |
| DEXAMETHASONE SODIUM PHOSPHATE | DEXAMETHASONE SODIUM PHOSPHATE | Eugia US LLC | ce7ad5a4-a9c5-42d6-87cc-ca16556208d2 | 2025-11-12 | Warnings, Adverse reactions | 1116927 1812194 AI9376Y64P |
| TopCare Pain Relief Maximum Strength | LIDOCAINE HYDROCHLORIDE | TOPCO ASSOCIATES | b0ae3a7c-52d1-4923-bd50-6bb3749006c8 | 2025-11-11 | Warnings | V13007Z41A |
| Comfortcaine | LIDOCAINE HCL | QS Key West Aloe, LLC | 831b7c11-e437-4e74-808e-c9c1eb8b82f6 | 2025-11-11 | Warnings | V13007Z41A |
| DermaNumb Analgesic | LIDOCAINE HCL | A.T.S. Laboratories, LLC | 0ea46890-45c3-4732-bc47-227f7c67daf1 | 2025-11-11 | Warnings | V13007Z41A |
| Derma Numb Pain Relief | LIDOCAINE HCL | A.T.S. Laboratories, LLC | 710991ae-8f82-4893-93a7-0ef3f815d132 | 2025-11-11 | Warnings | V13007Z41A |
| SODIUM CHLORIDE | SODIUM CHLORIDE | Hospira, Inc. | af6aebad-ef03-4d19-9a40-18e5a278b812 | 2025-11-11 | Warnings, Adverse reactions | 451W47IQ8X |
| Lidocaine Hydrochloride | LIDOCAINE HYDROCHLORIDE | Eugia US LLC | 5524cbfd-d6e6-42eb-aaa5-22495e0a86b6 | 2025-11-11 | Warnings, Adverse reactions | V13007Z41A |
| Jelcaine Sterile | LIDOCAINE HCL JELLY USP, 2% | Brookfield Pharmaceuticals, LLC | 1a39d1de-7aa2-3068-e063-6394a90aed85 | 2025-11-10 | Warnings | V13007Z41A |
| GuruNanda Pain Relief | LIDOCAINE HYDROCHLORIDE | GuruNanda, LLC. | 3ab6a133-8dca-e14e-e063-6394a90a85e7 | 2025-11-10 | Warnings | V13007Z41A |
| GURUNANDA NASAL SALINE | NASAL WASH | GURUNANDA LLC | 27dbf0bf-c273-2108-e063-6394a90a0a09 | 2025-11-10 | Warnings | 451W47IQ8X |
| Sensorcaine MPF | BUPIVACAINE HYDROCHLORIDE | Henry Schein, Inc. | 78c6789d-773e-4b26-90bd-34a6b6d730ce | 2025-11-07 | Boxed warning, Warnings, Adverse reactions | 7TQO7W3VT8 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.