NeuLumEX
- Product NDC
- 32909-926
- 11-digit product format
- 329090926
- Labeler code
- 32909
- Product ID
- 32909-926_6775f06f-8cae-429a-a6b3-41a7eead4e15
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Barium Sulfate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- E-Z-EM Canada Inc
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-12-01
- Marketing end
- 2022-03-31
- Substance
- BARIUM SULFATE
- Active strength
- 1 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 32909-926 | NEULUMEX (BARIUM SULFATE) SUSPENSION [E-Z-EM CANADA INC] | 4 | Legacy NDC | 20221118_f710edb6-e30d-e400-59a3-7ff437bebcd5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 32909-926-03 | 32909092603 | 450 mL in 1 BOTTLE, PLASTIC (32909-926-03) | 450 ml | 2019-12-01 | 0000-00-00 | No | No | Current |