Melphalan Hydrochloride
- Product NDC
- 25021-221
- 11-digit product format
- 250210221
- Labeler code
- 25021
- Product ID
- 25021-221_0f30bd90-ab7a-40b9-8581-ce62808dd957
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Melphalan Hydrochloride
- Dosage form
- KIT
- Route
- INTRAVENOUS
- Labeler
- Sagent Pharmaceuticals
- Application
- ANDA201379
- Marketing category
- ANDA
- Marketing start
- 2017-03-15
- Marketing end
- 2020-04-30
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 25021-221-60 | EA - Each | 25021-221 | e39a466b-f934-4e28-aff9-c0966ae99ef7 | 1 | 2017-05-03 |