Orange Book product
METHYLDOPA AND HYDROCHLOROTHIAZIDE 30MG;500MG
Orange Book ANDA 070543 · CHARTWELL RX SCIENCES LLC · Discontinued
Key facts
| Proprietary name | METHYLDOPA AND HYDROCHLOROTHIAZIDE |
|---|---|
| Active ingredients | HYDROCHLOROTHIAZIDE, METHYLDOPA |
| Strength | 30MG;500MG |
| Dosage form | TABLET |
| Route | ORAL |
| Application | ANDA070543 |
| Applicant holder | CHARTWELL RX SCIENCES LLC |
| Marketing status | Discontinued |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Jan 15, 1986 |
At a glance
- None Marketed products with the same ingredient, strength and form
- 1–9 Products in this application
- No Reference listed drug
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Orange Book products
The FDA Orange Book lists approved drug products with their therapeutic equivalence (TE) codes, reference listed drugs and marketing status. Products approved before 1982 show an approval date of Jan 1, 1982.