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ALKERAN
ALKERAN - 52609-0001-5 - (melphalan)
Drug Information of ALKERAN
| Product NDC: | 52609-0001 |
| Proprietary Name: | ALKERAN |
| Non Proprietary Name: | melphalan |
| Active Ingredient(s): | 2 mg/1 & nbsp; melphalan |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ALKERAN
| Product NDC: | 52609-0001 |
| Labeler Name: | Apo-Pharma USA, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA014691 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110101 |
Package Information of ALKERAN
| Package NDC: | 52609-0001-5 |
| Package Description: | 50 TABLET, FILM COATED in 1 BOTTLE (52609-0001-5) |
NDC Information of ALKERAN
| NDC Code | 52609-0001-5 |
| Proprietary Name | ALKERAN |
| Package Description | 50 TABLET, FILM COATED in 1 BOTTLE (52609-0001-5) |
| Product NDC | 52609-0001 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | melphalan |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110101 |
| Marketing Category Name | NDA |
| Labeler Name | Apo-Pharma USA, Inc |
| Substance Name | MELPHALAN |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Alkylating Activity [MoA],Alkylating Drug [EPC] |
