Midodrine Hydrochloride
- Product NDC
- 63629-7983
- 11-digit product format
- 636297983
- Labeler code
- 63629
- Product ID
- 63629-7983_97f2cbac-4f72-4cee-8817-faa2e827f306
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Midodrine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207169
- Marketing category
- ANDA
- Marketing start
- 2018-10-29
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7983-1 | 63629798301 | 30 TABLET in 1 BOTTLE (63629-7983-1) | 30 tablet | 2019-04-08 | 0000-00-00 | No | No | Current |