ELIGARD
- Product NDC
- 62935-222
- 11-digit product format
- 629350222
- Labeler code
- 62935
- Product ID
- 62935-222_e15a7cc7-e026-41cc-aaa1-6a6db8aa3a0f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Leuprolide Acetate
- Dosage form
- KIT
- Route
- SUBCUTANEOUS
- Labeler
- TOLMAR PHARMACEUTICALS INC.
- Application
- NDA021379
- Marketing category
- NDA
- Marketing start
- 2002-08-26
- 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 |
|---|---|---|---|---|---|
| 62935-222-05 | EA - Each | 62935-222 | fd6a78f6-99f0-44d3-b166-e9b001593af0 | 1 | 2014-11-05 |