HIPREX
- Product NDC
- 30698-477
- 11-digit product format
- 306980477
- Labeler code
- 30698
- Product ID
- 30698-477_1b35ea4d-8733-4f56-9143-168fc49e2247
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methenamine Hippurate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Validus Pharmaceuticals LLC
- Application
- NDA017681
- Marketing category
- NDA
- Marketing start
- 1976-09-09
- Marketing end
- 0000-00-00
- Substance
- METHENAMINE HIPPURATE
- Active strength
- 1 g/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 30698-477-01 | HIPREX | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 30698-477 | HIPREX (METHENAMINE HIPPURATE) TABLET [VALIDUS PHARMACEUTICALS LLC] | 1 | Legacy NDC, 1 package rows | 20220203_c8ddaa11-5753-46eb-8bd4-8f1d874a3ec4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 30698-477-01 | 30698047701 | 100 TABLET in 1 BOTTLE (30698-477-01) | 100 tablet | 1976-09-09 | 0000-00-00 | No | No | Current |