Varibar Thin Liquid
- Product NDC
- 32909-105
- Requested package NDC
- 32909-105-10
- 11-digit product format
- 329090105
- Labeler code
- 32909
- Product ID
- 32909-105_4836ad7d-79bf-4e86-a232-e260335bf82a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- barium sulfate
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- E-Z-EM Canada Inc
- Application
- NDA208036
- Marketing category
- NDA
- Marketing start
- 2019-04-30
- Substance
- BARIUM SULFATE
- Active strength
- .81 g/g
- Pharmacologic classes
- Radiographic Contrast Agent [EPC], X-Ray Contrast Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Orange Book products#
| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|---|---|---|---|---|---|---|
| N208036-001 | E-Z-HD | BARIUM SULFATE | 98% | FOR SUSPENSION / ORAL | RLD, RS | 2016-01-11 | |
| N208036-002 | E-Z-PAQUE | BARIUM SULFATE | 96% | FOR SUSPENSION / ORAL | RLD, RS | 2017-04-07 | |
| N208036-003 | E-Z-CAT DRY | BARIUM SULFATE | 40% | FOR SUSPENSION / ORAL | RLD | 2017-01-03 | |
| N208036-004 | VARIBAR THIN LIQUID | BARIUM SULFATE | 81% | FOR SUSPENSION / ORAL | RLD, RS | 2019-04-30 |
Observed Orange Book product history#
Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
| Captured | Edition | Application-product | Trade name | Strength | Dosage form / route | Product TE source text | RLD / RS | Approval date | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|
| 2026-08-01 22:54:32 | 2026-06 | N208036-001 | E-Z-HD | 98% | FOR SUSPENSION / ORAL | RLD, RS | 2016-01-11 | a50c72e98297… | |
| 2026-08-01 22:54:32 | 2026-06 | N208036-002 | E-Z-PAQUE | 96% | FOR SUSPENSION / ORAL | RLD, RS | 2017-04-07 | a50c72e98297… | |
| 2026-08-01 22:54:32 | 2026-06 | N208036-003 | E-Z-CAT DRY | 40% | FOR SUSPENSION / ORAL | RLD | 2017-01-03 | a50c72e98297… | |
| 2026-08-01 22:54:32 | 2026-06 | N208036-004 | VARIBAR THIN LIQUID | 81% | FOR SUSPENSION / ORAL | RLD, RS | 2019-04-30 | a50c72e98297… |
openFDA label cross-check#
Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| E-Z-Paque | BARIUM SULFATE | E-Z-EM Canada Inc | 7225868a-4037-c96a-44e3-3326d36cbedc | 2026-04-15 | Warnings, Adverse reactions | 208036 NDA208036 |
| Varibar Thin Liquid | BARIUM SULFATE | E-Z-EM Canada Inc | 59493c83-3941-cc84-cc37-a8696ae42873 | 2026-04-15 | Warnings, Adverse reactions | 208036 NDA208036 32909-105-10 32909-105 32909010510 |
| E-Z-HD | BARIUM SULFATE | E-Z-EM Canada Inc | a4330804-7179-472a-91cb-84bbd5079bb8 | 2026-04-15 | Warnings, Adverse reactions | 208036 NDA208036 |
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Varibar Thin Liquid
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BARIUM SULFATE | .81 g/g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 25BB7EKE2E | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 59493c83-3941-cc84-cc37-a8696ae42873 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 5dbf91a8-ec29-4ffc-807c-e3bae7fb67b1 | Product name | 1 | 20201123 |
| 85bed648-23ca-4804-98e6-e36aee999cad | Product name | 1 | 20190717 |
| 80de93b4-8a94-428d-beb7-d644353ee70b | Product name | 1 | 20180424 |
| eb4f7d5b-1286-40dc-b8bf-ad87ff51c688 | Product name | 1 | 20170522 |
| db8eb201-78c7-4590-8a71-fac0a539bd8c | Product name | 1 | 20170404 |
| 141092be-5eb5-452e-9f69-2d350aa70a87 | Product name | 1 | 20161208 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 32909-105-10 | Varibar Thin Liquid | 24 in 1 CASE | POWDER, FOR SUSPENSION | 24 | 7 | |
| 32909-105-10 | Varibar Thin Liquid | 148 g in 1 BOTTLE, PLASTIC | POWDER, FOR SUSPENSION | 148 | 7 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 32909-105-10 | GM - Gram | 32909-105 | 9f007af8-e649-443a-8038-3b3e179ca751 | 1 | 2014-07-02 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 32909-105-10 | 32909010510 | 24 BOTTLE, PLASTIC in 1 CASE (32909-105-10) / 148 g in 1 BOTTLE, PLASTIC | 2019-04-30 | 0000-00-00 | No | No | Current |