Hydralazine Hydrochloride
- Product NDC
- 71872-7050
- 11-digit product format
- 718727050
- Labeler code
- 71872
- Product ID
- 71872-7050_8959d188-3dbe-bf45-e053-2995a90afa2a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydralazine Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA203110
- Marketing category
- ANDA
- Marketing start
- 2015-06-29
- Marketing end
- 0000-00-00
- Substance
- HYDRALAZINE HYDROCHLORIDE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71872-7050 | HYDRALAZINE HYDROCHLORIDE INJECTION, SOLUTION [MEDICAL PURCHASING SOLUTIONS, LLC] | 2 | Legacy NDC | 20230531_895a2d19-79d2-9ff3-e053-2a95a90a1055.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71872-7050-1 | 71872705001 | 1 VIAL in 1 BAG (71872-7050-1) > 1 mL in 1 VIAL | 1 vial | 2018-06-20 | 0000-00-00 | No | No | Current |