Phenazopyridine Hydrochloride
- Product NDC
- 73028-202
- 11-digit product format
- 730280202
- Labeler code
- 73028
- Product ID
- 73028-202_8ab3d9f1-d0b3-42ff-8d25-ac6af52e6465
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- phenazopyridine hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Pageview Pharmaceuticals
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-12-01
- Marketing end
- 0000-00-00
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73028-202-01 | Phenazopyridine Hydrochloride | 100 in 1 BOTTLE | TABLET, COATED | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73028-202 | PHENAZOPYRIDINE HYDROCHLORIDE TABLET, COATED [PAGEVIEW PHARMACEUTICALS] | 3 | Legacy NDC, 1 package rows | 20220120_1f00a88f-25a6-4765-b1d9-8e4efc48f259.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73028-202-01 | 73028020201 | 100 TABLET, COATED in 1 BOTTLE (73028-202-01) | 2020-12-01 | 0000-00-00 | No | No | Current |