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 |
|---|---|---|---|---|---|---|
| Lidocaine Hydrochloride | LIDOCAINE HYDROCHLORIDE | Brookfield Pharmaceuticals, LLC. | e824ba5b-3289-5ad4-e053-2995a90acc20 | 2025-11-27 | Warnings, Adverse reactions | V13007Z41A |
| Walgreen Maximum strength pain relieving cleansing | BENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDE | WALGREENS CO. | 9a0443a2-f1a9-482d-b5ee-abe983e4ae32 | 2025-11-26 | Warnings | V13007Z41A |
| Walgreen Saline | NASAL | WALGREENS CO. | ee264d8b-0bb2-472a-907c-6a6291f154cd | 2025-11-26 | Warnings | 451W47IQ8X |
| Walgreen Pain Relieving Fragrance Free | LIDOCAINE HYDROCHLORIDE | WALGREENS CO. | 62c50ded-3fc9-4f65-9bfb-1144ed2e36b4 | 2025-11-26 | Warnings | V13007Z41A |
| Walgreens | FIRST AID ANTISEPTIC | Walgreens | ae731d28-8530-4dd0-aef7-b25f784b4777 | 2025-11-26 | Warnings | V13007Z41A |
| Thermacare Heat Therapy Max Strength Lidocaine Pain Relief Rollon | THERMACARE HEAT THERAPY MAX STRENGTH LIDOCAINE PAIN RELIEF ROLLON | Clarion Brands LLC | 4482d34d-eaca-5522-e063-6394a90a6afb | 2025-11-26 | Warnings | LKG8494WBH V13007Z41A |
| Lidocaine Hydrochloride | LIDOCAINE HYDROCHLORIDE | A-S Medication Solutions | 82b377ee-0e3e-4cb9-a644-f45434c21cca | 2025-11-26 | Warnings, Adverse reactions | V13007Z41A |
| ACD-A | ANTICOAGULANT CITRATE DEXTROSE SOLUTION FORMULA A | Fenwal, Inc. | ab19b011-0a51-4f04-9881-d9fc7cae95ae | 2025-11-25 | 1Q73Q2JULR | |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | beda35c3-9a8b-47ad-e053-2995a90a7b1b | 2025-11-24 | Warnings | 059QF0KO0R |
| Easy Care First Aid Eyewash | WATER | Tender Corporation | a070aac8-e6d2-ef10-e053-2a95a90aa5b1 | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | e07a064b-f680-405c-bbcd-24fac430951e | 2025-11-24 | Warnings | 059QF0KO0R |
| ULINE Eyewash | EYEWASH | Niagara Pharmaceuticals Inc. | 2d7f22d2-320b-6af1-e063-6294a90addc6 | 2025-11-24 | Warnings | 059QF0KO0R |
| Pur-Wash | EYEWASH | Niagara Pharmaceuticals, Inc. | 0d43b1c1-2699-37f1-e054-00144ff88e88 | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 777e1559-786f-8d54-e053-2991aa0aa98d | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 7289103a-5cbf-42f4-8848-e827149a43ca | 2025-11-24 | Warnings | 059QF0KO0R |
| Thermacare Heat Therapy Max Strength Lidocaine Pain Relief Gel | THERMACARE HEAT THERAPY MAX STRENGTH LIDOCAINE PAIN RELIEF GEL | Clarion Brands LLC | 445db02a-c8e8-6ebb-e063-6294a90a4301 | 2025-11-24 | Warnings | LKG8494WBH V13007Z41A |
| Natural Eyes Floaters Relief | CHELIDONIUM, EUPHRASIA, KALI SULPH, NATRUM MURIATICUM, PHOSPHORUS, PHYSOSTIGMA, SEPIA, SILICEA | TRP Company | 445dc831-195e-4b25-e063-6294a90a6efd | 2025-11-24 | Warnings | 451W47IQ8X |
| Lidocaine Hydrochloride | LIDOCAINE HYDROCHLORIDE | ProPharma Distribution | 42df73b0-20ee-d1aa-e063-6294a90aa275 | 2025-11-21 | Warnings, Adverse reactions | V13007Z41A |
| Eyewash Additive Concentrate | WATER AND PROPYLENE GLYCOL | Haws Corporation | dd168403-398c-41ff-b1df-d93e4ff39de3 | 2025-11-20 | Warnings | 059QF0KO0R |
| Vital Female Sexual Energy | AGNUS CASTUS, ARNICA MONTANA, AVENA SATIVA, CAULOPHYLLUM THALICTROIDES, CINCHONA OFFICINALIS, DAMIANA, HYPOPHYSIS SUIS, L-ARGININE, NATRUM MURIATICUM, ONOSMODIUM VIRGINIANUM, OOPHORINUM SUIS, PHOSPHORICUM ACIDUM, SEPIA, THUJA OCCIDENTALIS | Liddell Laboratories, Inc. | 1ca43c82-62b0-4191-81a4-27f7f94109dd | 2025-11-20 | Warnings | 451W47IQ8X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.