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Melphalan Hydrochloride
Melphalan Hydrochloride - 10139-321-01 - (Melphalan Hydrochloride)
Drug Information of Melphalan Hydrochloride
| Product NDC: | 10139-321 |
| Proprietary Name: | Melphalan Hydrochloride |
| Non Proprietary Name: | Melphalan Hydrochloride |
| Active Ingredient(s): | & nbsp; Melphalan Hydrochloride |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Melphalan Hydrochloride
| Product NDC: | 10139-321 |
| Labeler Name: | GeneraMedix Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090299 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091027 |
Package Information of Melphalan Hydrochloride
| Package NDC: | 10139-321-01 |
| Package Description: | 1 KIT in 1 CARTON (10139-321-01) * 10 mL in 1 VIAL, SINGLE-DOSE (10139-319-10) * 10 mL in 1 VIAL (10139-320-10) |
NDC Information of Melphalan Hydrochloride
| NDC Code | 10139-321-01 |
| Proprietary Name | Melphalan Hydrochloride |
| Package Description | 1 KIT in 1 CARTON (10139-321-01) * 10 mL in 1 VIAL, SINGLE-DOSE (10139-319-10) * 10 mL in 1 VIAL (10139-320-10) |
| Product NDC | 10139-321 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Melphalan Hydrochloride |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20091027 |
| Marketing Category Name | ANDA |
| Labeler Name | GeneraMedix Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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