Hydralazine Hydrochloride
- Product NDC
- 50090-2514
- 11-digit product format
- 500902514
- Labeler code
- 50090
- Product ID
- 50090-2514_7459b02f-b856-4754-9254-6635f12e8109
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydralazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA088468
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- Marketing end
- 0000-00-00
- Substance
- HYDRALAZINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2514-1 | Hydralazine Hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | | 18 |
| 50090-2514-2 | Hydralazine Hydrochloride | 180 in 1 BOTTLE | TABLET | 180 | | 18 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2514 | HYDRALAZINE HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 18 | Legacy NDC, 2 package rows | 20210416_f8a1b91c-ed4e-4fb4-b1c3-3d5a806fa501.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2514-1 | 50090251401 | 60 TABLET in 1 BOTTLE (50090-2514-1) | 60 tablet | 2017-02-13 | 0000-00-00 | No | No | Current |
| 50090-2514-2 | 50090251402 | 180 TABLET in 1 BOTTLE (50090-2514-2) | 180 tablet | 2016-10-14 | 0000-00-00 | No | No | Current |