Midodrine Hydrochloride
- Product NDC
- 0615-5647
- 11-digit product format
- 006155647
- Labeler code
- 0615
- Product ID
- 0615-5647_8da8c36d-8167-4eeb-a788-4d777bcff619
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Midodrine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA076577
- Marketing category
- ANDA
- Marketing start
- 2003-09-10
- Marketing end
- 0000-00-00
- Substance
- MIDODRINE HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#