Varibar Nectar
- Product NDC
- 32909-115
- 11-digit product format
- 329090115
- Labeler code
- 32909
- Product ID
- 32909-115_812e1e37-1e0f-831b-6a7e-60fdc7c43e82
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- barium sulfate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- E-Z-EM Canada Inc
- Application
- NDA208143
- Marketing category
- NDA
- Marketing start
- 2017-07-17
- Marketing end
- 2022-05-31
- Substance
- BARIUM SULFATE
- Active strength
- 400 mg/mL
- Pharmacologic classes
- Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 32909-115-00 | Varibar Nectar | 240 mL in 1 BOTTLE, PLASTIC | SUSPENSION | 240 | | 9 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 32909-115 | VARIBAR NECTAR (BARIUM SULFATE) SUSPENSION [E-Z-EM CANADA INC] | 7 | Legacy NDC, 1 package rows | 20241114_5e7045f7-b771-d8af-ce30-be95b2597c10.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 32909-115-00 | 32909011500 | 240 mL in 1 BOTTLE, PLASTIC (32909-115-00) | 240 ml | 2017-07-17 | 2022-05-31 | No | No | Current |