midodrine hydrochloride
- Product NDC
- 0615-8358
- 11-digit product format
- 006158358
- Labeler code
- 0615
- Product ID
- 0615-8358_5c7a2cc3-ab06-454f-856c-a482b3ece776
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- midodrine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA077746
- Marketing category
- ANDA
- Marketing start
- 2006-09-12
- Marketing end
- 2022-06-30
- 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
- 0000-00-00
- 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 |
|---|
| 0615-8358-39 | 00615835839 | 30 TABLET in 1 BLISTER PACK (0615-8358-39) | 30 tablet | 2020-10-08 | 2022-06-30 | No | No | Current |