Sodium Chloride
- Product NDC
- 81033-028
- 11-digit product format
- 810330028
- Labeler code
- 81033
- Product ID
- 81033-028_43cf75a9-e660-c580-e063-6394a90a0b87
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Chloride Tablets
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Kesin Pharma Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2025-03-01
- Substance
- SODIUM CHLORIDE
- Active strength
- 1000 mg/1
- 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 | 1000 mg/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 |
|---|
| 81033-028-01 | Sodium Chloride | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81033-028 | SODIUM CHLORIDE (SODIUM CHLORIDE TABLETS) TABLET [KESIN PHARMA CORPORATION] | 1 | Current NDC, 1 package rows | 20250328_2f107592-10c5-ef3b-e063-6394a90a7c0a.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 |
|---|
| 81033-028-01 | 81033002801 | 100 TABLET in 1 BOTTLE (81033-028-01) | 100 tablet | 2025-03-01 | No | No | Current |