DailyMed label
Bisoprolol Fumarate and Hydrochlorothiazide
DailyMed label · Edenbridge Pharmaceuticals LLC. · version 11
Key facts
| Product | Bisoprolol Fumarate and Hydrochlorothiazide |
|---|---|
| Labeler | Edenbridge Pharmaceuticals LLC. |
| Document type | Human Prescription Drug Label |
| Active ingredients | BISOPROLOL FUMARATE, HYDROCHLOROTHIAZIDE |
| Active ingredient UNIIs | 0J48LPH2TH, UR59KN573L |
| Application number | 212678 |
| Route | ORAL |
| NDC package codes | 42799-920-30, 42799-920-01, 42799-920-02, 42799-921-30, 42799-921-01, 42799-921-02, 42799-922-30, 42799-922-01, 42799-922-02 |
| Effective date | Aug 28, 2026 |
| Set ID | 295532b5-65c8-40c3-8d27-cfd334d12802 |
At a glance
- 1–9 NDC package codes
- 1–9 Active ingredients
- None Manufacturing establishments listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About DailyMed drug labels
DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.
Source: U.S. National Library of Medicine (NLM), DailyMed · Source date: