Wound Debridement Kit
- Product NDC
- 69263-920
- 11-digit product format
- 692630920
- Labeler code
- 69263
- Product ID
- 69263-920_542a42c6-cc33-087c-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- wound debridement kit
- Dosage form
- KIT
- Route
- TOPICAL
- Labeler
- Oaklock, LLC
- Application
- ANDA088803
- Marketing category
- ANDA
- Marketing start
- 2015-11-18
- 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 |
|---|---|---|---|---|---|
| 69263-920-01 | EA - Each | 69263-920 | 112ea939-95be-4f35-8564-1d25e92e2247 | 1 | 2017-08-11 |