Lidolog Kit
- Product NDC
- 80425-0244
- 11-digit product format
- 804250244
- Labeler code
- 80425
- Product ID
- 80425-0244_2a9ae6d7-049a-3bd5-e063-6394a90a651e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lidocaine, kenalog, povidone iodine
- Dosage form
- KIT
- Route
- EPIDURAL; INFILTRATION; INTRA-ARTICULAR; INTRAMUSCULAR; TOPICAL
- Labeler
- Advanced Rx Pharmacy of Tennessee, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2023-05-15
- 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 |
|---|
| 80425-0244-1 | 80425024401 | 1 KIT in 1 CARTON (80425-0244-1) * 25 VIAL in 1 CARTON (70121-1049-5) / 1 mL in 1 VIAL * .9 mL in 1 PACKET (67777-419-02) * 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-164-02) / 2 mL in 1 VIAL, SINGLE-DOSE | 1 kit | 2023-05-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lidolog Kit | Advanced Rx Pharmacy of Tennessee, LLC | Advanced Rx Pharmacy of Tennssee, LLC | 2024-12-31 | HUMAN PRESCRIPTION DRUG LABEL | 2 |