MIDODRINE HYDROCHLORIDE
- Product NDC
- 42291-616
- 11-digit product format
- 422910616
- Labeler code
- 42291
- Product ID
- 42291-616_6f3eea1e-d5c4-1854-e053-2a91aa0ae07b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MIDODRINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE, Inc.
- Application
- ANDA076449
- Marketing category
- ANDA
- Marketing start
- 2011-03-03
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record