Dexamethasone Sodium Phosphate
- Product NDC
- 76420-555
- 11-digit product format
- 764200555
- Labeler code
- 76420
- Product ID
- 76420-555_f87f3d2b-033d-ea7a-e053-6394a90ac766
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone Sodium Phosphate
- Dosage form
- INJECTION
- Route
- INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE
- Labeler
- Asclemed USA, Inc.
- Application
- ANDA084282
- Marketing category
- ANDA
- Marketing start
- 1975-07-15
- Substance
- DEXAMETHASONE SODIUM PHOSPHATE
- Active strength
- 4 mg/mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dexamethasone Sodium Phosphate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DEXAMETHASONE SODIUM PHOSPHATE | 4 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | AI9376Y64P |
| Rxcui | 1812194 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76420-555-01 | Dexamethasone Sodium Phosphate | 1 mL in 1 VIAL | INJECTION | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76420-555 | DEXAMETHASONE SODIUM PHOSPHATE INJECTION [ASCLEMED USA, INC.] | 1 | Current NDC, 1 package rows | 20230406_2d96d5e8-00bf-406b-b345-f1c31865fe94.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 76420-555-01 | 76420055501 | 1 mL in 1 VIAL (76420-555-01) | 1 ml | 2023-04-04 | No | No | Historical |