Bacteriostatic Water
- Product NDC
- 70518-1236
- 11-digit product format
- 705181236
- Labeler code
- 70518
- Product ID
- 70518-1236_e5558c4c-db09-31ec-e053-2995a90add7c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bacteriostatic Water
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- REMEDYREPACK INC.
- Application
- NDA018802
- Marketing category
- NDA
- Marketing start
- 2018-06-04
- Marketing end
- 0000-00-00
- Substance
- WATER
- Active strength
- 1 mL/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70518-1236-0 | 70518123600 | 25 VIAL, MULTI-DOSE in 1 TRAY (70518-1236-0) > 30 mL in 1 VIAL, MULTI-DOSE (70518-1236-1) | 2018-06-04 | 0000-00-00 | No | No | Current |