Sodium Nitroprusside
- Product NDC
- 71839-120
- 11-digit product format
- 718390120
- Labeler code
- 71839
- Product ID
- 71839-120_01841345-bed3-458f-8e99-911fbd286512
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Nitroprusside
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- BE Pharmaceuticals Inc.
- Application
- ANDA214971
- Marketing category
- ANDA
- Marketing start
- 2021-07-12
- 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 |
|---|
| 71839-120-01 | Sodium Nitroprusside | 2 mL in 1 VIAL | INJECTION | 2 | | 1 |
| 71839-120-01 | 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 |
|---|
| 71839-120 | SODIUM NITROPRUSSIDE INJECTION [BE PHARMACEUTICALS INC.] | 1 | Current NDC, Legacy NDC, 2 package rows | 20210724_01841345-bed3-458f-8e99-911fbd286512.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71839-120-01 | 71839012001 | 1 VIAL in 1 CARTON (71839-120-01) / 2 mL in 1 VIAL | 1 vial | 2021-07-12 | 0000-00-00 | No | No | Current |