TriXylitral
- Product NDC
- 69621-707
- 11-digit product format
- 696210707
- Labeler code
- 69621
- Product ID
- 69621-707_23a932ee-9371-4242-a3be-ac6207141d9f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium, Lidocaine Hydrochloride
- Dosage form
- KIT
- Labeler
- Shoreline Pharmaceuticals
- Application
- ANDA202769
- Marketing category
- ANDA
- Marketing start
- 2018-01-15
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 69621-707-00 | EA - Each | 69621-707 | da2551e0-2bc3-4308-88ac-5cb837e0e275 | 1 | 2018-08-13 |