Nat Mur
- Product NDC
- 44911-0159
- 11-digit product format
- 449110159
- Labeler code
- 44911
- Product ID
- 44911-0159_2b87acf5-dc1b-4fc9-8697-e11b09a440b4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Natrum Muriaticum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-05-19
- Marketing end
- 2028-11-28
- Substance
- SODIUM CHLORIDE
- Active strength
- 30 [hp_C]/mL
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nat Mur
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM CHLORIDE | 30 [hp_C]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 451W47IQ8X |
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 |
|---|
| 44911-0159-1 | Nat Mur | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 44911-0159 | NAT MUR (NATRUM MURIATICUM) LIQUID [ENERGIQUE, INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20241031_39c4cb25-e70f-4d5a-b7b6-1b62527aa4f3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 44911-0159-1 | 44911015901 | 30 mL in 1 BOTTLE, DROPPER (44911-0159-1) | 30 ml | 2015-05-19 | 2028-11-28 | No | No | Current |