POTASSIUM IODIDE
- Product NDC
- 72162-2423
- 11-digit product format
- 721622423
- Labeler code
- 72162
- Product ID
- 72162-2423_1312d1fa-6c50-4d5b-99d0-dcd9c0fe8a13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- POTASSIUM IODIDE
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2021-12-29
- Substance
- POTASSIUM IODIDE
- Active strength
- 1 g/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- POTASSIUM IODIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM IODIDE | 1 g/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 1C4QK22F9J |
| Rxcui | 312541 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2423-2 | POTASSIUM IODIDE | 237 mL in 1 BOTTLE | SOLUTION | 237 | | 100 |
| 72162-2423-3 | POTASSIUM IODIDE | 30 mL in 1 BOTTLE, WITH APPLICATOR | SOLUTION | 30 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2423 | POTASSIUM IODIDE SOLUTION [BRYANT RANCH PREPACK] | 100 | Current NDC, 2 package rows | 20241113_90cf3abb-c6d4-4004-8ae2-f528260a72f4.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 |
|---|
| 72162-2423-2 | 72162242302 | 237 mL in 1 BOTTLE (72162-2423-2) | 237 ml | 2024-11-11 | No | No | Historical |
| 72162-2423-3 | 72162242303 | 30 mL in 1 BOTTLE, WITH APPLICATOR (72162-2423-3) | 30 ml | 2024-11-11 | No | No | Historical |