Phenazopyridine Hydrochloride
- Product NDC
- 63629-8986
- 11-digit product format
- 636298986
- Labeler code
- 63629
- Product ID
- 63629-8986_adb78c3f-3b58-49c3-8940-87172eb06f53
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2011-08-23
- Marketing end
- 0000-00-00
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 200 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 |
|---|
| 63629-8986-1 | 63629898601 | 10 TABLET in 1 BOTTLE (63629-8986-1) | 10 tablet | 2021-12-07 | 0000-00-00 | No | No | Current |