NDC 42571-332 – Methenamine Hippurate
Methenamine Hippurate 1000 mg/1 · Tablet · Oral
Product NDC42571-332
Product details
- Brand name
- Methenamine Hippurate
- Generic name
- Methenamine Hippurate
- Labeler
- Micro Labs Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA212172
- Marketed since
- August 15, 2019
- Listing expires
- December 31, 2026
Active ingredients
- Methenamine Hippurate 1000 mg/1
Uses, dosage, side effects and warnings for Methenamine Hippurate →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 42571-332-01 | 100 TABLET in 1 BOTTLE (42571-332-01) | Aug 15, 2019 |
| 42571-332-23 | 80 TABLET in 1 CARTON (42571-332-23) | Aug 15, 2019 |
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