NDC 71205-906 – Midodrine Hydrochloride
Midodrine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC71205-906
Product details
- Brand name
- Midodrine Hydrochloride
- Generic name
- Midodrine hydrochloride
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207849
- Marketed since
- October 15, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- alpha-Adrenergic Agonist
Active ingredients
- Midodrine Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Midodrine Hydrochloride →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71205-906-00 | 100 TABLET in 1 BOTTLE, PLASTIC (71205-906-00) | Jul 20, 2021 |
| 71205-906-11 | 1000 TABLET in 1 BOTTLE, PLASTIC (71205-906-11) | Jul 20, 2021 |
| 71205-906-30 | 30 TABLET in 1 BOTTLE, PLASTIC (71205-906-30) | Jul 20, 2021 |
| 71205-906-55 | 500 TABLET in 1 BOTTLE, PLASTIC (71205-906-55) | Jul 20, 2021 |
| 71205-906-60 | 60 TABLET in 1 BOTTLE, PLASTIC (71205-906-60) | Jul 20, 2021 |
| 71205-906-72 | 120 TABLET in 1 BOTTLE, PLASTIC (71205-906-72) | Jul 20, 2021 |
| 71205-906-90 | 90 TABLET in 1 BOTTLE, PLASTIC (71205-906-90) | Jul 20, 2021 |
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