0074-3023 : K-tab 1500 mg/1 Oral Tablet, Film Coated, Extended Release
NDC: | 0074-3023 |
Labeler: | Abbvie Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | K-tab |
Dosage Form: | Oral Tablet, Film Coated, Extended Release |
Application #: | NDA018279 |
Rev. Date: |
Appearance:
Markings: | KTAB |
Shapes: |
Oval |
Colors: |
White |
Size (mm): | 20 |
Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. |
NDC Package Codes:
- 0074-3023-13: 100 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (0074‑3023‑13)
- 0074-3023-30: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (0074‑3023‑30)
- 0074-3023-53: 500 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (0074‑3023‑53)
- 0074-3023-90: 90 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (0074‑3023‑90)
Active Ingredients:
- Potassium Chloride
Dosage Strength:
- 1500 mg
Inactive Ingredients:
- Castor Oil
- Silicon Dioxide
- Magnesium Stearate
- Paraffin
- Titanium Dioxide
- Vanillin
- Alpha-tocopherol
- Ethylcelluloses
- Polyvinyl Acetate
Pharmaceutical 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]
Related Products:
Based on records with the same trade name.- 0074-3058 K-tab 600 mg Oral Tablet, Film Coated, Extended Release by Abbvie Inc.
- 0074-3278 K-tab 750 mg Oral Tablet, Film Coated, Extended Release by Abbvie Inc.
- 0074-7804 K-tab 10 Meq Extended Release Tablet by Abbvie Inc.
- 43353-790 K-tab 10 Meq Extended Release Tablet by Aphena Pharma Solutions - Tennessee, Inc.
- 53808-0277 K-tab 10 Meq Extended Release Tablet by State of Florida Doh Central Pharmacy
- 70518-0220 K-tab 750 mg Oral Tablet, Film Coated, Extended Release by Remedyrepack Inc.
NDC QR Code
Scan the QR code below to easily reference this data in the future:< Prev: 0074-3020Next: 0074-3025 >
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.