Vanilla SilQ MD
- Product NDC
- 69307-4096
- 11-digit product format
- 693074096
- Labeler code
- 69307
- Product ID
- 69307-4096_b8a2bb97-7fd4-6075-e053-2a95a90acb13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Barium Sulfate For Suspension
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL; RECTAL
- Labeler
- Genus Medical Technologies, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2015-06-01
- Marketing end
- 0000-00-00
- Substance
- BARIUM SULFATE
- Active strength
- 96 g/100g
- Pharmacologic classes
- Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69307-4096-2 | Vanilla SilQ MD | 176 g in 1 BOTTLE, PLASTIC | POWDER, FOR SUSPENSION | 176 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69307-4096 | VANILLA SILQ MD (BARIUM SULFATE FOR SUSPENSION) POWDER, FOR SUSPENSION [GENUS MEDICAL TECHNOLOGIES, LLC] | 4 | Legacy NDC, 1 package rows | 20210112_1282f284-2419-0249-e054-00144ff8d46c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69307-4096-2 | 69307409602 | 176 g in 1 BOTTLE, PLASTIC (69307-4096-2) | 176 g | 2015-06-01 | 0000-00-00 | No | No | Current |