Phenazopyridine Hydrochloride
- Product NDC
- 42291-548
- 11-digit product format
- 422910548
- Labeler code
- 42291
- Product ID
- 42291-548_b0ee6600-f91c-379f-e053-2995a90a6696
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2015-10-07
- Marketing end
- 0000-00-00
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
Dataset, Scope, Product NDC table| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|
| excluded product | product | 42291-548 | | D | Discontinued by firm | | 2026-07-31 |
| excluded package | package | 42291-548 | 42291-548-90 | D | Discontinued by firm | | 2026-07-31 |
DailyMed Socrata Ingredients#