MIDODRINE HYDROCHLORIDE
- Product NDC
- 0615-8443
- 11-digit product format
- 006158443
- Labeler code
- 0615
- Product ID
- 0615-8443_7e7d850a-1230-45d7-9945-3331413dab14
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MIDODRINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA214734
- Marketing category
- ANDA
- Marketing start
- 2021-01-22
- Marketing end
- 0000-00-00
- Substance
- MIDODRINE HYDROCHLORIDE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0615-8443-39 | 00615844339 | 30 TABLET in 1 BLISTER PACK (0615-8443-39) | 30 tablet | 2022-12-07 | 0000-00-00 | No | No | Current |