BACTERIOSTATIC SODIUM CHLORIDE
- Product NDC
- 70518-1318
- 11-digit product format
- 705181318
- Labeler code
- 70518
- Product ID
- 70518-1318_c1c1533c-2961-1dc8-e053-2a95a90a0649
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM CHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- REMEDYREPACK INC.
- Application
- NDA018800
- Marketing category
- NDA
- Marketing start
- 2020-06-19
- Marketing end
- 0000-00-00
- Substance
- SODIUM CHLORIDE
- Active strength
- 9 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 70518-1318-1 | 70518131801 | 25 VIAL, MULTI-DOSE in 1 TRAY (70518-1318-1) > 30 mL in 1 VIAL, MULTI-DOSE (70518-1318-0) | 2020-06-19 | 0000-00-00 | No | No | Current |