Methenamine Hippurate
- Product NDC
- 69315-210
- 11-digit product format
- 693150210
- Labeler code
- 69315
- Product ID
- 69315-210_ad5daa79-2752-4c6e-a042-18a49e140222
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methenamine Hippurate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Leading Pharma, LLC
- Application
- NDA017681
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-06-03
- Marketing end
- 0000-00-00
- Substance
- METHENAMINE HIPPURATE
- Active strength
- 1 g/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69315-210-01 | 69315021001 | 100 TABLET in 1 BOTTLE (69315-210-01) | 100 tablet | 2016-06-03 | 0000-00-00 | No | No | Current |