Phenazopyridine Hydrochloride
- Product NDC
- 0440-8069
- 11-digit product format
- 004408069
- Labeler code
- 0440
- Product ID
- 0440-8069_da51b9f5-e1c7-4764-adb3-993437cfc8fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Liberty Pharmaceuticals, Inc.
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record