NDC 71335-2750 – Phenazopyridine Hydrochloride
Phenazopyridine Hydrochloride 200 mg/1 · Tablet · Oral
Product NDC71335-2750
Product details
- Brand name
- Phenazopyridine Hydrochloride
- Generic name
- Phenazopyridine
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketed since
- February 1, 2011
- Listing expires
- December 31, 2026
Active ingredients
- Phenazopyridine Hydrochloride 200 mg/1
Uses, dosage, side effects and warnings for Phenazopyridine Hydrochloride →
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2750-1 | 9 TABLET in 1 BOTTLE (71335-2750-1) | Jul 24, 2025 |
| 71335-2750-2 | 20 TABLET in 1 BOTTLE (71335-2750-2) | Jul 24, 2025 |
| 71335-2750-3 | 30 TABLET in 1 BOTTLE (71335-2750-3) | Jul 24, 2025 |
| 71335-2750-4 | 10 TABLET in 1 BOTTLE (71335-2750-4) | Jul 24, 2025 |
| 71335-2750-5 | 15 TABLET in 1 BOTTLE (71335-2750-5) | Jul 24, 2025 |
| 71335-2750-6 | 6 TABLET in 1 BOTTLE (71335-2750-6) | Jul 24, 2025 |
| 71335-2750-7 | 90 TABLET in 1 BOTTLE (71335-2750-7) | Jul 24, 2025 |
| 71335-2750-8 | 12 TABLET in 1 BOTTLE (71335-2750-8) | Jul 24, 2025 |
| 71335-2750-9 | 18 TABLET in 1 BOTTLE (71335-2750-9) | Jul 24, 2025 |
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