NDC 62756-368 – Metoprolol Tartrate and Hydrochlorothiazide
Metoprolol Tartrate 100 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Oral
Product NDC62756-368
Product details
- Brand name
- Metoprolol Tartrate and Hydrochlorothiazide
- Generic name
- Metoprolol Tartrate and Hydrochlorothiazide
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA090654
- Marketed since
- April 1, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Thiazide Diuretic; beta-Adrenergic Blocker
Active ingredients
- Metoprolol Tartrate 100 mg/1
- Hydrochlorothiazide 25 mg/1
Uses, dosage, side effects and warnings for Metoprolol Tartrate and Hydrochlorothiazide →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 62756-368-08 | 100 TABLET in 1 BOTTLE (62756-368-08) | Apr 1, 2022 |
| 62756-368-18 | 1000 TABLET in 1 BOTTLE (62756-368-18) | Apr 1, 2022 |
| 62756-368-83 | 30 TABLET in 1 BOTTLE (62756-368-83) | Apr 1, 2022 |
| 62756-368-88 | 100 TABLET in 1 BOTTLE (62756-368-88) | Apr 1, 2022 |
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- 62756-369 Metoprolol Tartrate 100 mg/1; Hydrochlorothiazide 50 mg/1 · Tablet · Sun Pharmaceutical Industries, Inc.