BRUC HOMO
- Product NDC
- 43742-1729
- 11-digit product format
- 437421729
- Labeler code
- 43742
- Product ID
- 43742-1729_d09f61f8-b7f4-49be-bcb5-e2e5353beb80
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Brucella Melitensis
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-10-02
- Substance
- BRUCELLA MELITENSIS
- Active strength
- 18 [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BRUC HOMO
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BRUCELLA MELITENSIS | 18 [hp_C]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | OQF85710LZ |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43742-1729-1 | BRUC HOMO | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43742-1729 | BRUC HOMO (BRUCELLA MELITENSIS) LIQUID [DESERET BIOLOGICALS, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20240425_916e818d-3f85-4020-ae9b-755d348576be.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-1729-1 | 43742172901 | 30 mL in 1 BOTTLE, DROPPER (43742-1729-1) | 30 ml | 2020-10-02 | 0000-00-00 | No | No | Current |