Potassium Chloride
- Product NDC
- 42291-679
- 11-digit product format
- 422910679
- Labeler code
- 42291
- Product ID
- 42291-679_4871a1e2-6b72-31fb-e063-6394a90a7297
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA077419
- Marketing category
- ANDA
- Marketing start
- 2013-03-05
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Potassium Chloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM CHLORIDE | 750 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 660YQ98I10 |
| Rxcui | 312504, 315183 |
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 |
|---|
| 42291-679-50 | Potassium Chloride | 500 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 500 | | 9 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| POTASSIUM CHLORIDE | ACTIVE INGREDIENT | 660YQ98I10 | POTASSIUM CHLORIDE (POTASSIUM CHLORIDE) CAPSULE, EXTENDED RELEASE [AVKARE, INC.] | 1 | |
| POTASSIUM CATION | ACTIVE MOIETY | 295O53K152 | POTASSIUM CHLORIDE (POTASSIUM CHLORIDE) CAPSULE, EXTENDED RELEASE [AVKARE, INC.] | 1 | |
| ETHYLCELLULOSES | INACTIVE INGREDIENT | 7Z8S9VYZ4B | POTASSIUM CHLORIDE (POTASSIUM CHLORIDE) CAPSULE, EXTENDED RELEASE [AVKARE, INC.] | 1 | |
| FD&C BLUE NO. 1 | INACTIVE INGREDIENT | H3R47K3TBD | POTASSIUM CHLORIDE (POTASSIUM CHLORIDE) CAPSULE, EXTENDED RELEASE [AVKARE, INC.] | 1 | |
| FD&C RED NO. 40 | INACTIVE INGREDIENT | WZB9127XOA | POTASSIUM CHLORIDE (POTASSIUM CHLORIDE) CAPSULE, EXTENDED RELEASE [AVKARE, INC.] | 1 | |
| GELATIN | INACTIVE INGREDIENT | 2G86QN327L | POTASSIUM CHLORIDE (POTASSIUM CHLORIDE) CAPSULE, EXTENDED RELEASE [AVKARE, INC.] | 1 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | POTASSIUM CHLORIDE (POTASSIUM CHLORIDE) CAPSULE, EXTENDED RELEASE [AVKARE, INC.] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | POTASSIUM CHLORIDE (POTASSIUM CHLORIDE) CAPSULE, EXTENDED RELEASE [AVKARE, INC.] | 1 | |
| TRIACETIN | INACTIVE INGREDIENT | XHX3C3X673 | POTASSIUM CHLORIDE (POTASSIUM CHLORIDE) CAPSULE, EXTENDED RELEASE [AVKARE, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42291-679 | POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [AVKARE] | 8 | Current NDC, Legacy NDC, 1 package rows | 20220908_755a4a08-04ff-d7d1-a6fc-b8aeff3ae2c6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-679-50 | 42291067950 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42291-679-50) | 2013-03-05 | 0000-00-00 | No | No | Current |