Details for New Drug Application (NDA): 016080
✉ Email this page to a colleague
NDA 016080 describes MANNITOL 5% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.12%, which is a drug marketed by B Braun and is included in one NDA. Additional details are available on the MANNITOL 5% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.12% profile page.
The generic ingredient in MANNITOL 5% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.12% is mannitol. There are eighteen drug master file entries for this compound. Ten suppliers are listed for this compound. Additional details are available on the mannitol profile page.
The generic ingredient in MANNITOL 5% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.12% is mannitol. There are eighteen drug master file entries for this compound. Ten suppliers are listed for this compound. Additional details are available on the mannitol profile page.
Summary for 016080
| Tradename: | MANNITOL 5% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.12% |
| Applicant: | B Braun |
| Ingredient: | mannitol |
| Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 016080
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE;INJECTION | Strength | 5GM/100ML | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE;INJECTION | Strength | 10GM/100ML | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | No | |||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE;INJECTION | Strength | 15GM/100ML | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | No | |||||
Complete Access Available with Subscription
