Phenazopyridine HCl 200mg
- Product NDC
- 70934-812
- 11-digit product format
- 709340812
- Labeler code
- 70934
- Product ID
- 70934-812_c0964dfe-e9b4-b371-e053-2a95a90a251f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2021-01-05
- 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 |
|---|
| 70934-812-06 | 70934081206 | 6 TABLET in 1 BOTTLE, PLASTIC (70934-812-06) | 6 tablet | 2021-04-22 | 0000-00-00 | No | No | Current |
| 70934-812-10 | 70934081210 | 10 TABLET in 1 BOTTLE, PLASTIC (70934-812-10) | 10 tablet | 2021-01-05 | 0000-00-00 | No | No | Current |