Sodium Chloride
- Product NDC
- 65282-1505
- 11-digit product format
- 652821505
- Labeler code
- 65282
- Product ID
- 65282-1505_447bf261-1a3a-2da1-e063-6394a90a7537
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Spectra Medical Deviecs, LLC
- Application
- ANDA206171
- Marketing category
- ANDA
- Marketing start
- 2017-07-21
- Substance
- SODIUM CHLORIDE
- Active strength
- 9 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sodium Chloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM CHLORIDE | 9 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 451W47IQ8X |
| Rxcui | 1807637, 1807646 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 65282-1505-1 | Sodium Chloride | 5 in 1 TRAY | INJECTION, SOLUTION | 5 | | 17 |
| 65282-1505-1 | Sodium Chloride | 5 in 1 CARTON | INJECTION, SOLUTION | 5 | | 17 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65282-1505 | SODIUM CHLORIDE INJECTION, SOLUTION [SPECTRA MEDICAL DEVIECS, LLC] | 16 | Current NDC, Legacy NDC, 2 package rows | 20240113_7e316d21-d6ad-4976-bd90-268fd7e51361.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65282-1505-1 | 65282150501 | 5 TRAY in 1 CARTON (65282-1505-1) / 5 AMPULE in 1 TRAY / 5 mL in 1 AMPULE | 5 tray | 2017-07-21 | 0000-00-00 | No | No | Current |