Sodium Chloride
- Product NDC
- 71872-7082
- 11-digit product format
- 718727082
- Labeler code
- 71872
- Product ID
- 71872-7082_c3f8e83c-4fb8-91da-e053-2a95a90abd63
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- NDA018803
- Marketing category
- NDA
- Marketing start
- 2005-02-28
- 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 |
|---|
| 71872-7082-1 | 71872708201 | 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7082-1) > 10 mL in 1 VIAL, SINGLE-DOSE | 2021-01-01 | 0000-00-00 | No | No | Current |