NDC 71205-904 – Midodrine Hydrochloride
Midodrine Hydrochloride 2.5 mg/1 · Tablet · Oral
Product NDC71205-904
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 2.5 mg/1
Uses, dosage, side effects and warnings for Midodrine Hydrochloride →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71205-904-00 | 100 TABLET in 1 BOTTLE, PLASTIC (71205-904-00) | Jul 20, 2021 |
| 71205-904-11 | 1000 TABLET in 1 BOTTLE, PLASTIC (71205-904-11) | Jul 20, 2021 |
| 71205-904-30 | 30 TABLET in 1 BOTTLE, PLASTIC (71205-904-30) | Jul 20, 2021 |
| 71205-904-55 | 500 TABLET in 1 BOTTLE, PLASTIC (71205-904-55) | Jul 20, 2021 |
| 71205-904-60 | 60 TABLET in 1 BOTTLE, PLASTIC (71205-904-60) | Jul 20, 2021 |
| 71205-904-72 | 120 TABLET in 1 BOTTLE, PLASTIC (71205-904-72) | Jul 20, 2021 |
| 71205-904-90 | 90 TABLET in 1 BOTTLE, PLASTIC (71205-904-90) | Jul 20, 2021 |
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- 60687-387 Midodrine Hydrochloride 2.5 mg/1 · Tablet · American Health Packaging
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