Details for New Drug Application (NDA): 011835
✉ Email this page to a colleague
NDA 011835 describes HYDRODIURIL, which is a drug marketed by Merck and is included in one NDA. Additional details are available on the HYDRODIURIL profile page.
The generic ingredient in HYDRODIURIL is hydrochlorothiazide. There are thirty-two drug master file entries for this compound. Forty-five suppliers are listed for this compound. Additional details are available on the hydrochlorothiazide profile page.
The generic ingredient in HYDRODIURIL is hydrochlorothiazide. There are thirty-two drug master file entries for this compound. Forty-five suppliers are listed for this compound. Additional details are available on the hydrochlorothiazide profile page.
Summary for 011835
| Tradename: | HYDRODIURIL |
| Applicant: | Merck |
| Ingredient: | hydrochlorothiazide |
| Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 011835
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | Yes | |||||
Profile for product number 006
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | Yes | |||||
Profile for product number 007
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | Yes | |||||
Complete Access Available with Subscription
