Phenazopyridine Hydrochloride
- Product NDC
- 63629-2028
- 11-digit product format
- 636292028
- Labeler code
- 63629
- Product ID
- 63629-2028_450a7220-490c-4750-939a-4bb8ea50afb5
- 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
- 100 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 63629-2028-1 | 63629202801 | 100 TABLET in 1 BOTTLE (63629-2028-1) | 100 tablet | 2021-02-01 | 0000-00-00 | No | No | Current |