Potassium Chloride
- Product NDC
- 64725-0600
- 11-digit product format
- 647250600
- Labeler code
- 64725
- Product ID
- 64725-0600_cc2bbbc5-dd33-4821-a97a-cc7452815998
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- TYA Pharmaceuticals
- Application
- NDA018279
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2011-02-22
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 64725-0600-1 | Potassium Chloride | 30 in 1 CONTAINER | TABLET, FILM COATED, EXTENDED RE | 30 | | 2 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| POTASSIUM CHLORIDE | ACTIVE INGREDIENT | 660YQ98I10 | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 2 | |
| POTASSIUM CATION | ACTIVE MOIETY | 295O53K152 | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 2 | |
| .ALPHA.-TOCOPHEROL | INACTIVE INGREDIENT | H4N855PNZ1 | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 2 | |
| CASTOR OIL | INACTIVE INGREDIENT | D5340Y2I9G | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 2 | |
| D&C YELLOW NO. 10 | INACTIVE INGREDIENT | 35SW5USQ3G | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 2 | |
| ETHYLCELLULOSES | INACTIVE INGREDIENT | 7Z8S9VYZ4B | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 2 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 2 | |
| PARAFFIN | INACTIVE INGREDIENT | I9O0E3H2ZE | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 2 | |
| POLYVINYL ACETATE | INACTIVE INGREDIENT | 32K497ZK2U | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 2 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 2 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 2 | |
| VANILLIN | INACTIVE INGREDIENT | CHI530446X | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 2 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64725-0600 | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [TYA PHARMACEUTICALS] | 2 | Legacy NDC, 1 package rows | 20141110_eb4939b8-1d90-4e56-8e59-40733d700744.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64725-0600-1 | 64725060001 | 30 in 1 CONTAINER | Historical |