Midodrine HCl
- Product NDC
- 63739-556
- 11-digit product format
- 637390556
- Labeler code
- 63739
- Product ID
- 63739-556_59c94b8a-0973-4025-88a3-8ce658f20dd7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Midodrine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Corporation
- Application
- ANDA076514
- Marketing category
- ANDA
- Marketing start
- 2003-09-11
- 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
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record