HYDRALAZINE HYDROCHLORIDE
- Product NDC
- 0404-9986
- 11-digit product format
- 004049986
- Labeler code
- 0404
- Product ID
- 0404-9986_9a710d4a-a51e-484b-902e-13092ef9fb82
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydralazine hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Henry Schein, Inc.
- Application
- ANDA040730
- Marketing category
- ANDA
- Marketing start
- 2022-10-14
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0404-9986-20 | 00404998620 | 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9986-20) > 1 mL in 1 VIAL, SINGLE-DOSE | 2022-10-14 | 0000-00-00 | No | No | Current |