K-Tab
- Product NDC
- 0074-3278
- 11-digit product format
- 000743278
- Labeler code
- 0074
- Product ID
- 0074-3278_2babd1a6-739a-462b-bb4e-bf9fc8b477ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- AbbVie Inc.
- Application
- NDA018279
- Marketing category
- NDA
- Marketing start
- 2017-06-01
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0074-3278-13 | 00074327813 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0074-3278-13) | 2017-06-01 | 0000-00-00 | No | No | Current |
| 0074-3278-19 | 00074327819 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0074-3278-19) | 2017-06-01 | 0000-00-00 | No | No | Current |