Midodrine Hydrochloride
- Product NDC
- 71335-2174
- 11-digit product format
- 713352174
- Labeler code
- 71335
- Product ID
- 71335-2174_e5452ec7-c37e-40ab-8c89-7d9766b94e12
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Midodrine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212543
- Marketing category
- ANDA
- Marketing start
- 2019-08-19
- 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
- 2023-12-31
- 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 |
|---|
| 71335-2174-1 | 71335217401 | 30 TABLET in 1 BOTTLE (71335-2174-1) | 30 tablet | 2022-10-10 | 0000-00-00 | No | No | Current |