Vanilla SilQ
- Product NDC
- 69307-1024
- 11-digit product format
- 693071024
- Labeler code
- 69307
- Product ID
- 69307-1024_b8a2c0df-591c-73c8-e053-2a95a90ac408
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Barium Sulfate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Genus Medical Technologies, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2014-10-27
- Marketing end
- 0000-00-00
- Substance
- BARIUM SULFATE
- Active strength
- 21 mg/mL
- 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 |
|---|
| 69307-1024-2 | Vanilla SilQ | 450 mL in 1 BOTTLE, PLASTIC | SUSPENSION | 450 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69307-1024 | VANILLA SILQ (BARIUM SULFATE) SUSPENSION [GENUS MEDICAL TECHNOLOGIES, LLC] | 4 | Legacy NDC, 1 package rows | 20210112_05f1030d-1a9c-05df-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 |
|---|
| 69307-1024-2 | 69307102402 | 450 mL in 1 BOTTLE, PLASTIC (69307-1024-2) | 450 ml | 2014-10-27 | 0000-00-00 | No | No | Current |