Sodium Nitroprusside
- Product NDC
- 70700-126
- 11-digit product format
- 707000126
- Labeler code
- 70700
- Product ID
- 70700-126_e0e8d0aa-672f-8821-87cc-3ccaf3f5315a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Nitroprusside Injection
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- Xiromed, LLC.
- Application
- ANDA211277
- Marketing category
- ANDA
- Marketing start
- 2021-02-11
- Marketing end
- 0000-00-00
- Substance
- SODIUM NITROPRUSSIDE
- Active strength
- 50 mg/2mL
- Pharmacologic classes
- Vasodilation [PE],Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70700-126-92 | Sodium Nitroprusside | 1 in 1 CARTON | INJECTION, SOLUTION, CONCENTRATE | 1 | | 2 |
| 70700-126-92 | Sodium Nitroprusside | 2 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION, CONCENTRATE | 2 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70700-126 | SODIUM NITROPRUSSIDE (SODIUM NITROPRUSSIDE INJECTION) INJECTION, SOLUTION, CONCENTRATE [XIROMED, LLC.] | 2 | Legacy NDC, 2 package rows | 20210212_90f4f18f-eb6a-d700-6ec4-c4961f6ab49c.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 |
|---|
| 70700-126-92 | 70700012692 | 1 VIAL, SINGLE-DOSE in 1 CARTON (70700-126-92) > 2 mL in 1 VIAL, SINGLE-DOSE | 2021-02-11 | 0000-00-00 | No | No | Current |