Midodrine hydrochloride
- Product NDC
- 70771-1595
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Midodrine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA213055
- Marketing category
- ANDA
- Substance
- MIDODRINE HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 70771-1595-1 | 100 TABLET in 1 BOTTLE (70771-1595-1) | 2020-09-17 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Midodrine Hydrochloride Tablets, USP Rx Only | Zydus Lifesciences Limited | 2023-11-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |