Zeyocaine
- Product NDC
- 69621-821
- 11-digit product format
- 696210821
- Labeler code
- 69621
- Product ID
- 69621-821_dfa240db-ef4b-4d10-8196-ac578e47ce15
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lidocaine, isopropyl alcohol
- Dosage form
- KIT
- Route
- TOPICAL
- Labeler
- Shoreline Pharmaceuticals, Inc.
- Application
- ANDA205318
- Marketing category
- ANDA
- Marketing start
- 2016-09-30
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 69621-821-00 | EA - Each | 69621-821 | 026e8797-7412-413d-bc57-cc51e6d3277d | 1 | 2017-03-06 |