SODIUM CHLORIDE
- Product NDC
- 77333-846
- 11-digit product format
- 773330846
- Labeler code
- 77333
- Product ID
- 77333-846_4f5246bf-4e78-d23a-e063-6294a90aa63b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM CHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Gendose Pharmaceuticals, LLC
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-05-01
- Substance
- SODIUM CHLORIDE
- Active strength
- 1 g/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SODIUM CHLORIDE
- Brand name suffix
- 1 GRAM
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM CHLORIDE | 1 g/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 451W47IQ8X |
| Rxcui | 313009 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 77333-846-10 | SODIUM CHLORIDE1 GRAM | 100 in 1 BOX | TABLET | 100 | | 1 |
| 77333-846-25 | SODIUM CHLORIDE1 GRAM | 10 in 1 BLISTER PACK | TABLET | 10 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 77333-846-10 | 77333084610 | 100 BLISTER PACK in 1 BOX (77333-846-10) / 10 TABLET in 1 BLISTER PACK (77333-846-25) | 100 blister pack | 2026-05-01 | No | No | Current |
| 77333-846-25 | 77333084625 | 10 in 1 BLISTER PACK | | | | | Historical |