UristatUTI Relief Pak
- Product NDC
- 0440-8065
- 11-digit product format
- 004408065
- Labeler code
- 0440
- Product ID
- 0440-8065_5a4f76e9-f914-4e6f-b218-abf3ab5460c6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Phenazopyridine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Liberty Pharmaceuticals, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2015-04-29
- Marketing end
- 0000-00-00
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 95 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 0440-8065-01 | UristatUTI Relief PakUTI Relief Pak | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
| 0440-8065-05 | UristatUTI Relief PakUTI Relief Pak | 500 in 1 BOTTLE | TABLET | 500 | | 2 |
| 0440-8065-30 | UristatUTI Relief PakUTI Relief Pak | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 0440-8065-69 | UristatUTI Relief PakUTI Relief Pak | 96 in 1 BLISTER PACK | TABLET | 96 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0440-8065 | URISTATUTI RELIEF PAK UTI RELIEF PAK (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET [LIBERTY PHARMACEUTICALS, INC.] | 2 | Legacy NDC, 4 package rows | 20161019_f6e24576-e90c-451e-b2f8-261b61a00fcc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 0440-8065-01 | 00440806501 | 100 in 1 BOTTLE | Historical |
| 0440-8065-05 | 00440806505 | 500 in 1 BOTTLE | Historical |
| 0440-8065-30 | 00440806530 | 30 in 1 BOTTLE | Historical |
| 0440-8065-69 | 00440806569 | 96 in 1 BLISTER PACK | Historical |