SODIUM NITROPRUSSIDE
- Product NDC
- 55150-320
- 11-digit product format
- 551500320
- Labeler code
- 55150
- Product ID
- 55150-320_41e11afb-5fa4-4212-889d-1092dbd0702a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM NITROPRUSSIDE
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- AuroMedics Pharma LLC
- Application
- ANDA211934
- Marketing category
- ANDA
- Marketing start
- 2020-12-10
- 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 |
|---|
| 55150-320-01 | SODIUM NITROPRUSSIDE | 2 mL in 1 VIAL, SINGLE-DOSE | INJECTION | 2 | | 1 |
| 55150-320-01 | SODIUM NITROPRUSSIDE | 1 in 1 CARTON | INJECTION | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55150-320 | SODIUM NITROPRUSSIDE INJECTION [AUROMEDICS PHARMA LLC] | 1 | Current NDC, Legacy NDC, 2 package rows | 20201215_41e11afb-5fa4-4212-889d-1092dbd0702a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55150-320-01 | 55150032001 | 1 VIAL, SINGLE-DOSE in 1 CARTON (55150-320-01) / 2 mL in 1 VIAL, SINGLE-DOSE | 2020-12-10 | 0000-00-00 | No | No | Current |