SODIUM ACETATE
- Product NDC
- 69784-230
- 11-digit product format
- 697840230
- Labeler code
- 69784
- Product ID
- 69784-230_ef736af9-9b51-44da-e053-2995a90af28d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM ACETATE
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- Woodward Pharma Services LLC
- Application
- ANDA214805
- Marketing category
- ANDA
- Marketing start
- 2021-06-01
- Marketing end
- 0000-00-00
- Substance
- SODIUM ACETATE
- Active strength
- 164 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69784-230 | SODIUM ACETATE INJECTION, SOLUTION, CONCENTRATE [WOODWARD PHARMA SERVICES LLC] | 6 | Legacy NDC | 20231104_dfa26fd6-53dd-499c-8c40-fd0623d2c8f1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69784-230-20 | 69784023020 | 50 mL in 1 VIAL, PHARMACY BULK PACKAGE (69784-230-20) | 50 ml | 2021-06-01 | 0000-00-00 | No | No | Current |