HYDRALAZINE HYDROCHLORIDE
- Product NDC
- 21695-695
- 11-digit product format
- 216950695
- Labeler code
- 21695
- Product ID
- 21695-695_d0a368ef-a524-4eb4-b984-5ee1d9d5a93d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydralazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA040901
- Marketing category
- ANDA
- Marketing start
- 2008-09-12
- Marketing end
- 0000-00-00
- Substance
- HYDRALAZINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 21695-695-90 | HYDRALAZINE HYDROCHLORIDE | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-695 | HYDRALAZINE HYDROCHLORIDE TABLET [REBEL DISTRIBUTORS CORP] | 2 | Legacy NDC, 1 package rows | 20111118_e9888fe1-a2ed-41b5-b5dd-df7fff3fad37.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-695-90 | 21695069590 | 90 in 1 BOTTLE | Historical |