Potassium Phosphates
- Product NDC
- 63323-086
- 11-digit product format
- 633230086
- Labeler code
- 63323
- Product ID
- 63323-086_230d1e93-063b-4349-a1e8-ee1ce9312b80
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- POTASSIUM PHOSPHATE, MONOBASIC and POTASSIUM PHOSPHATE, DIBASIC
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2000-08-08
- Marketing end
- 2022-11-30
- Substance
- POTASSIUM PHOSPHATE, MONOBASIC; POTASSIUM PHOSPHATE, DIBASIC
- Active strength
- 224 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 63323-086-05 | 63323008605 | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-086-05) > 5 mL in 1 VIAL, SINGLE-DOSE | 2000-08-08 | 2022-10-31 | No | No | Current |
| 63323-086-15 | 63323008615 | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-086-15) > 15 mL in 1 VIAL, SINGLE-DOSE | 2000-08-08 | 2022-05-31 | No | No | Current |
| 63323-086-50 | 63323008650 | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-086-50) > 50 mL in 1 VIAL, SINGLE-DOSE | 2000-08-08 | 2022-11-30 | No | No | Current |