Phenazopyridine Hydrochloride
- Product NDC
- 63629-7701
- 11-digit product format
- 636297701
- Labeler code
- 63629
- Product ID
- 63629-7701_6e69f597-4132-428a-b7f0-93c9f120d29b
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7701-1 | 63629770101 | 10 TABLET in 1 BOTTLE (63629-7701-1) | 10 tablet | 2018-07-06 | 0000-00-00 | No | No | Current |
| 63629-7701-2 | 63629770102 | 12 TABLET in 1 BOTTLE (63629-7701-2) | 12 tablet | 2018-07-06 | 0000-00-00 | No | No | Current |
| 63629-7701-3 | 63629770103 | 20 TABLET in 1 BOTTLE (63629-7701-3) | 20 tablet | 2018-07-06 | 0000-00-00 | No | No | Current |
| 63629-7701-4 | 63629770104 | 90 TABLET in 1 BOTTLE (63629-7701-4) | 90 tablet | 2018-07-06 | 0000-00-00 | No | No | Current |
| 63629-7701-5 | 63629770105 | 100 TABLET in 1 BOTTLE (63629-7701-5) | 100 tablet | 2018-07-06 | 0000-00-00 | No | No | Current |