Sodium Chloride
- Product NDC
- 70369-010
- 11-digit product format
- 703690010
- Labeler code
- 70369
- Product ID
- 70369-010_2ce80e1e-5259-596d-e063-6294a90add01
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Citragen Pharmaceuticals Inc
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-07-20
- Substance
- SODIUM CHLORIDE
- Active strength
- 500 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
- Brand name suffix
- Normal Salt
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM CHLORIDE | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 451W47IQ8X |
| Rxcui | 2387545 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70369-010-09 | 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 |
|---|
| 70369-010 | SODIUM CHLORIDE NORMAL SALT (SODIUM CHLORIDE) TABLET [CITRAGEN PHARMACEUTICALS INC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250131_aae783b2-18fe-69ca-e053-2a95a90a0800.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 |
|---|
| 70369-010-09 | 70369001009 | 200 TABLET in 1 BOTTLE (70369-010-09) | 200 tablet | 2020-07-20 | 0000-00-00 | No | No | Current |