Sodium Chloride
- Product NDC
- 52584-186
- 11-digit product format
- 525840186
- Labeler code
- 52584
- Product ID
- 52584-186_b95cb3c1-cee0-41a6-b9ac-7103570f9739
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Chloride
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA088912
- Marketing category
- ANDA
- Marketing start
- 2019-07-03
- Marketing end
- 2024-03-31
- Substance
- SODIUM CHLORIDE
- Active strength
- 9 mg/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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-186-01 | 52584018601 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-186-01) > 10 mL in 1 VIAL, SINGLE-DOSE | 2019-07-03 | 0000-00-00 | No | No | Current |