NDC 71335-0770 – Hydrochlorothiazide
Hydrochlorothiazide 12.5 mg/1 · Capsule · Oral
Product NDC71335-0770
Product details
- Brand name
- Hydrochlorothiazide
- Generic name
- Hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA078164
- Marketed since
- September 19, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- Thiazide Diuretic
Active ingredients
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Hydrochlorothiazide →
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0770-1 | 30 CAPSULE in 1 BOTTLE (71335-0770-1) | Apr 13, 2018 |
| 71335-0770-2 | 10 CAPSULE in 1 BOTTLE (71335-0770-2) | May 7, 2018 |
| 71335-0770-3 | 90 CAPSULE in 1 BOTTLE (71335-0770-3) | Apr 10, 2018 |
| 71335-0770-4 | 100 CAPSULE in 1 BOTTLE (71335-0770-4) | Oct 1, 2018 |
| 71335-0770-5 | 60 CAPSULE in 1 BOTTLE (71335-0770-5) | Oct 15, 2019 |
| 71335-0770-6 | 120 CAPSULE in 1 BOTTLE (71335-0770-6) | Aug 13, 2019 |
| 71335-0770-7 | 7 CAPSULE in 1 BOTTLE (71335-0770-7) | Apr 11, 2019 |
| 71335-0770-8 | 15 CAPSULE in 1 BOTTLE (71335-0770-8) | Apr 11, 2019 |
| 71335-0770-9 | 14 CAPSULE in 1 BOTTLE (71335-0770-9) | Oct 7, 2024 |
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