Midodrine HCl
- Product NDC
- 0185-0043
- 11-digit product format
- 001850043
- Labeler code
- 0185
- Product ID
- 0185-0043_b82311c6-0dfa-4d39-9db1-33e03163a2b5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Midodrine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Eon Labs, Inc.
- Application
- ANDA076514
- Marketing category
- ANDA
- Marketing start
- 2003-09-11
- Marketing end
- 2021-09-30
- 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
- 0000-00-00
- 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 |
|---|
| 0185-0043-01 | 00185004301 | 100 TABLET in 1 BOTTLE (0185-0043-01) | 100 tablet | 2003-09-11 | 2021-07-31 | No | No | Current |
| 0185-0043-05 | 00185004305 | 500 TABLET in 1 BOTTLE (0185-0043-05) | 500 tablet | 2003-09-11 | 2021-09-30 | No | No | Current |