SODIUM CHLORIDE
- Product NDC
- 52584-109
- 11-digit product format
- 525840109
- Labeler code
- 52584
- Product ID
- 52584-109_27c4834c-bf0d-49f2-97bd-73d3a7fc5550
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sodium chloride
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA212248
- Marketing category
- ANDA
- Marketing start
- 2021-07-28
- Marketing end
- 2024-03-31
- Substance
- SODIUM CHLORIDE
- Active strength
- 4 meq/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-109-01 | 52584010901 | 1 VIAL in 1 BAG (52584-109-01) > 30 mL in 1 VIAL | 1 vial | 2021-07-28 | 2024-03-31 | No | No | Current |