Sodium nitroprusside
- Product NDC
- 70121-1189
- 11-digit product format
- 701211189
- Labeler code
- 70121
- Product ID
- 70121-1189_68b15b81-486f-4f89-9f88-9ac103767767
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium nitroprusside
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Amneal Pharmaceuticals LLC
- Application
- ANDA209493
- Marketing category
- ANDA
- Marketing start
- 2017-11-07
- Substance
- SODIUM NITROPRUSSIDE
- Active strength
- 25 mg/mL
- 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 | 25 mg/mL |
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 |
|---|
| 70121-1189-1 | Sodium nitroprusside | 1 in 1 CARTON | INJECTION | 1 | | 10 |
| 70121-1189-1 | Sodium nitroprusside | 2 mL in 1 VIAL, SINGLE-DOSE | INJECTION | 2 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70121-1189 | SODIUM NITROPRUSSIDE INJECTION [AMNEAL PHARMACEUTICALS LLC] | 10 | Current NDC, Legacy NDC, 2 package rows | 20240808_2fa687a2-10e7-45ae-953a-9d63564c2908.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 |
|---|
| 70121-1189-1 | 70121118901 | 1 VIAL, SINGLE-DOSE in 1 CARTON (70121-1189-1) / 2 mL in 1 VIAL, SINGLE-DOSE | 2017-11-07 | 0000-00-00 | No | No | Current |