Phenazopyridine Hydrochloride
- Product NDC
- 70154-115
- 11-digit product format
- 701540115
- Labeler code
- 70154
- Product ID
- 70154-115_9e53c8cb-c19e-524f-e053-2a95a90a9442
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Monarch PCM, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-09-23
- Marketing end
- 0000-00-00
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record