Midodrine Hydrochloride
- Product NDC
- 63629-6928
- 11-digit product format
- 636296928
- Labeler code
- 63629
- Product ID
- 63629-6928_e4528fcf-bcc1-4af6-b253-6f91ea788b82
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- midodrine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076577
- Marketing category
- ANDA
- Marketing start
- 2003-09-11
- Marketing end
- 0000-00-00
- Substance
- MIDODRINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6928-1 | 63629692801 | 30 TABLET in 1 BOTTLE (63629-6928-1) | 30 tablet | 2016-03-02 | 0000-00-00 | No | No | Current |
| 63629-6928-2 | 63629692802 | 90 TABLET in 1 BOTTLE (63629-6928-2) | 90 tablet | 2016-03-02 | 0000-00-00 | No | No | Current |