Phenazopyridine Hydrochloride
- Product NDC
- 63629-1001
- 11-digit product format
- 636291001
- Labeler code
- 63629
- Product ID
- 63629-1001_8d23387f-dfb5-4be3-9bc1-890f3e4201af
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2011-02-01
- Marketing end
- 0000-00-00
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 200 mg/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 |
|---|
| 63629-1001-1 | 63629100101 | 100 TABLET in 1 BOTTLE (63629-1001-1) | 100 tablet | 2020-12-07 | 0000-00-00 | No | No | Current |
| 63629-1001-2 | 63629100102 | 12 TABLET in 1 BOTTLE (63629-1001-2) | 12 tablet | 2020-12-07 | 0000-00-00 | No | No | Current |
| 63629-1001-3 | 63629100103 | 30 TABLET in 1 BOTTLE (63629-1001-3) | 30 tablet | 2020-12-07 | 0000-00-00 | No | No | Current |
| 63629-1001-4 | 63629100104 | 90 TABLET in 1 BOTTLE (63629-1001-4) | 90 tablet | 2020-12-07 | 0000-00-00 | No | No | Current |