K Phos
- Product NDC
- 68151-2193
- 11-digit product format
- 681512193
- Labeler code
- 68151
- Product ID
- 68151-2193_01e77301-afcb-421b-b2c3-58ad1fbef7b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Phosphate, Monobasic
- Dosage form
- TABLET, SOLUBLE
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1977-03-29
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM PHOSPHATE, MONOBASIC
- Active strength
- 500 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 68151-2193-0 | K Phos Original | 1 in 1 PACKAGE | TABLET, SOLUBLE | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2193 | K PHOS ORIGINAL (POTASSIUM PHOSPHATE, MONOBASIC) TABLET, SOLUBLE [CARILION MATERIALS MANAGEMENT] | 2 | Legacy NDC, 1 package rows | 20160617_0d128959-ddfe-4255-a5fe-6e6c09764d82.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2193-0 | 68151219300 | 1 in 1 PACKAGE | Historical |