Nacellate Solution 0.9% - 100mL
- Product NDC
- 70529-021
- 11-digit product format
- 705290021
- Labeler code
- 70529
- Product ID
- 70529-021_4140bb42-ede3-4fcd-a43e-671f403b5874
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- IT3 Medical LLC
- Application
- NDA017464
- Marketing category
- NDA
- Marketing start
- 2017-03-01
- Marketing end
- 0000-00-00
- Substance
- SODIUM CHLORIDE
- Active strength
- 9 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70529-021-01 | Nacellate Solution 0.9% - 100mL | 100 mL in 1 CONTAINER | INJECTION, SOLUTION | 100 | | 4 |
| 70529-021-01 | Nacellate Solution 0.9% - 100mL | 1 in 1 PACKAGE | INJECTION, SOLUTION | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70529-021 | NACELLATE SOLUTION 0.9% - 100ML (SODIUM CHLORIDE) INJECTION, SOLUTION [IT3 MEDICAL LLC] | 4 | Legacy NDC, 2 package rows | 20220302_5664d350-2ab2-4e50-9c57-fd42f987c5dd.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 |
|---|
| 70529-021-01 | 70529002101 | 1 CONTAINER in 1 PACKAGE (70529-021-01) > 100 mL in 1 CONTAINER | 1 container | 2017-03-01 | 0000-00-00 | No | No | Current |