DoubleDex Kit
- Product NDC
- 80425-0232
- 11-digit product format
- 804250232
- Labeler code
- 80425
- Product ID
- 80425-0232_2a9b1617-60d2-f8ce-e063-6294a90ab02c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone Sodium Phosphate, Povidine Iodine
- Dosage form
- KIT
- Route
- INTRAMUSCULAR; INTRAVENOUS; TOPICAL
- Labeler
- Advanced Rx Pharmacy of Tennessee, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2023-05-12
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 80425-0232-1 | 80425023201 | 1 KIT in 1 CARTON (80425-0232-1) * .9 mL in 1 PACKET (67777-419-02) * 5 mL in 1 POUCH * 25 VIAL in 1 TRAY (63323-506-01) / 1 mL in 1 VIAL | 1 kit | 2023-05-12 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| DoubleDex Kit | Advanced Rx Pharmacy of Tennessee, LLC | 2024-12-31 | HUMAN PRESCRIPTION DRUG LABEL | 2 |