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Soltamox
Soltamox - 13632-123-01 - (tamoxifen citrate)
Drug Information of Soltamox
| Product NDC: | 13632-123 |
| Proprietary Name: | Soltamox |
| Non Proprietary Name: | tamoxifen citrate |
| Active Ingredient(s): | 10 mg/5mL & nbsp; tamoxifen citrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Soltamox
| Product NDC: | 13632-123 |
| Labeler Name: | Rosemont Pharmaceuticals Ltd |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021807 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20121001 |
Package Information of Soltamox
| Package NDC: | 13632-123-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (13632-123-01) > 150 mL in 1 BOTTLE |
NDC Information of Soltamox
| NDC Code | 13632-123-01 |
| Proprietary Name | Soltamox |
| Package Description | 1 BOTTLE in 1 CARTON (13632-123-01) > 150 mL in 1 BOTTLE |
| Product NDC | 13632-123 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tamoxifen citrate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20121001 |
| Marketing Category Name | NDA |
| Labeler Name | Rosemont Pharmaceuticals Ltd |
| Substance Name | TAMOXIFEN CITRATE |
| Strength Number | 10 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Estrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA] |
