NDC 71335-2321 – Phenazopyridine Hydrochloride
Phenazopyridine Hydrochloride 200 mg/1 · Tablet · Oral
Product NDC71335-2321
Product details
- Brand name
- Phenazopyridine Hydrochloride
- Generic name
- Phenazopyridine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketed since
- October 19, 2023
- 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 |
|---|---|---|
| 71335-2321-1 | 9 TABLET in 1 BOTTLE (71335-2321-1) | Jan 4, 2024 |
| 71335-2321-2 | 20 TABLET in 1 BOTTLE (71335-2321-2) | Jan 4, 2024 |
| 71335-2321-3 | 30 TABLET in 1 BOTTLE (71335-2321-3) | Jan 4, 2024 |
| 71335-2321-4 | 10 TABLET in 1 BOTTLE (71335-2321-4) | Jan 4, 2024 |
| 71335-2321-5 | 15 TABLET in 1 BOTTLE (71335-2321-5) | Jan 4, 2024 |
| 71335-2321-6 | 6 TABLET in 1 BOTTLE (71335-2321-6) | Jan 4, 2024 |
| 71335-2321-7 | 90 TABLET in 1 BOTTLE (71335-2321-7) | Jan 4, 2024 |
| 71335-2321-8 | 12 TABLET in 1 BOTTLE (71335-2321-8) | Jan 4, 2024 |
| 71335-2321-9 | 18 TABLET in 1 BOTTLE (71335-2321-9) | Jan 4, 2024 |
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