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Sclerosol
Sclerosol - 63256-100-30 - (Talc)
Drug Information of Sclerosol
| Product NDC: | 63256-100 |
| Proprietary Name: | Sclerosol |
| Non Proprietary Name: | Talc |
| Active Ingredient(s): | 4 g/25g & nbsp; Talc |
| Administration Route(s): | INTRAPLEURAL |
| Dosage Form(s): | AEROSOL, POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sclerosol
| Product NDC: | 63256-100 |
| Labeler Name: | Bryan Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020587 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130630 |
Package Information of Sclerosol
| Package NDC: | 63256-100-30 |
| Package Description: | 1 CANISTER in 1 POUCH (63256-100-30) > 30 g in 1 CANISTER |
NDC Information of Sclerosol
| NDC Code | 63256-100-30 |
| Proprietary Name | Sclerosol |
| Package Description | 1 CANISTER in 1 POUCH (63256-100-30) > 30 g in 1 CANISTER |
| Product NDC | 63256-100 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Talc |
| Dosage Form Name | AEROSOL, POWDER |
| Route Name | INTRAPLEURAL |
| Start Marketing Date | 20130630 |
| Marketing Category Name | NDA |
| Labeler Name | Bryan Corp |
| Substance Name | TALC |
| Strength Number | 4 |
| Strength Unit | g/25g |
| Pharmaceutical Classes |
