Sodium Nitroprusside
- Product NDC
- 75907-290
- 11-digit product format
- 759070290
- Labeler code
- 75907
- Product ID
- 75907-290_b246076f-49e6-6a0d-e065-9b3f853adb2d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Nitroprusside
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Dr.Reddy's Laboratories Inc.,
- Application
- ANDA210114
- Marketing category
- ANDA
- Marketing start
- 2025-12-01
- Substance
- SODIUM NITROPRUSSIDE
- Active strength
- 50 mg/2mL
- Pharmacologic classes
- Vasodilation [PE], Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sodium Nitroprusside
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM NITROPRUSSIDE | 50 mg/2mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | EAO03PE1TC |
| Rxcui | 240793 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 75907-290-11 | Sodium Nitroprusside | 2 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 2 | | 1 |
| 75907-290-11 | Sodium Nitroprusside | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 75907-290-11 | 75907029011 | 1 VIAL, SINGLE-DOSE in 1 CARTON (75907-290-11) / 2 mL in 1 VIAL, SINGLE-DOSE | 2025-12-01 | No | No | Current |