Sclerosol
- Product NDC
- 63256-100
- 11-digit product format
- 632560100
- Labeler code
- 63256
- Product ID
- 63256-100_05246011-b7f0-40a3-ac67-b1bd8d23edac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Talc
- Dosage form
- AEROSOL, POWDER
- Route
- INTRAPLEURAL
- Labeler
- Bryan Corp
- Application
- NDA020587
- Marketing category
- NDA
- Marketing start
- 2013-06-30
- Marketing end
- 0000-00-00
- Substance
- TALC
- Active strength
- 4 g/25g
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63256-100-30 | Sclerosol | 1 in 1 POUCH | AEROSOL, POWDER | 1 | | 4 |
| 63256-100-30 | Sclerosol | 30.0 g in 1 CANISTER | AEROSOL, POWDER | 30.0 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63256-100 | SCLEROSOL (TALC) AEROSOL, POWDER [BRYAN CORP] | 4 | Legacy NDC, 2 package rows | 20130630_c89eb8fd-6c31-4f8b-8103-1f559424eda1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 63256-100-30 | 63256010030 | 1 in 1 POUCH | Historical |