E-Z-Paque
- Product NDC
- 32909-186
- 11-digit product format
- 329090186
- Labeler code
- 32909
- Product ID
- 32909-186_2865005d-5345-6eab-6d31-24e97d1c4fdd
- 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
- 2017-03-01
- Marketing end
- 2021-10-31
- Substance
- BARIUM SULFATE
- Active strength
- 1 g/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 Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 32909-186 | E-Z-PAQUE (BARIUM SULFATE) SUSPENSION [E-Z-EM CANADA INC] | 7 | Legacy NDC | 20201101_2ecea1ab-66c8-4eb0-8503-6d6b41b51328.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 32909-186-02 | 32909018602 | 1 BOTTLE, PLASTIC in 1 CARTON (32909-186-02) > 355 mL in 1 BOTTLE, PLASTIC | 2017-03-01 | 2021-10-31 | No | No | Current |