Sodium Chloride
- Product NDC
- 55681-333
- 11-digit product format
- 556810333
- Labeler code
- 55681
- Product ID
- 55681-333_4e507f5a-9254-a674-e063-6394a90aceb7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- TWIN MED LLC
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-10-01
- 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
- Normal Salt
- 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 |
|---|
| 55681-333-02 | Sodium ChlorideNormal Salt | 200 in 1 BOTTLE | TABLET | 200 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55681-333 | SODIUM CHLORIDE NORMAL SALT (SODIUM CHLORIDE) TABLET [TWIN MED LLC] | 1 | Current NDC, 1 package rows | 20241011_10230c8a-e5e5-44f1-b41d-80930899d6b9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 55681-333-02 | 55681033302 | 200 TABLET in 1 BOTTLE (55681-333-02) | 200 tablet | 2024-10-01 | No | No | Historical |