Phenazopyridine Hydrochloride
- Product NDC
- 55700-283
- 11-digit product format
- 557000283
- Labeler code
- 55700
- Product ID
- 55700-283_3c9abab4-c560-484e-bdaf-1aa64bbcdd16
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- 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
- 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 |
|---|
| 55700-283-06 | 55700028306 | 6 TABLET in 1 BOTTLE (55700-283-06) | 6 tablet | 2015-08-31 | 0000-00-00 | No | No | Current |