Phenazopyridine Hydrochloride
- Product NDC
- 64205-520
- 11-digit product format
- 642050520
- Labeler code
- 64205
- Product ID
- 64205-520_a54651f7-ec26-4eff-8a65-c1b89cc42f28
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ReadyMeds
- 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
- 2017-12-31
- 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 |
|---|
| 64205-520-09 | Phenazopyridine Hydrochloride | 9 in 1 BOTTLE | TABLET | 9 | | 5 |
| 64205-520-15 | Phenazopyridine Hydrochloride | 15 in 1 PACKAGE | TABLET | 15 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64205-520 | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [READYMEDS] | 5 | Legacy NDC, 2 package rows | 20140506_32918084-20f5-4050-b94e-09c0dd72e910.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64205-520-09 | 64205052009 | 9 in 1 BOTTLE | Historical |
| 64205-520-15 | 64205052015 | 15 in 1 PACKAGE | Historical |