Register entry
- Registered sites
- 0
- Active NDC listings
- 4
- Labeller names
- 2
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
44 active NDC listings: 4 bulk ingredient. By marketing category: BULK INGREDIENT 4.
| Dosage form | NDCs |
|---|---|
| powder | 4 |
| Route | NDCs |
|---|
| Labeller name on the listing | NDCs |
|---|---|
| merck & cie | 3 |
| merck & cie | 1 |
Catalogue
Marketed products
4| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | Bisoprolol Hemifumarate | powder | 54784-027BULK INGREDIENT |
| - | CALCIUM FOLINATE AMORPHOUS | powder | 54784-010BULK INGREDIENT |
| - | Calcium Folinate Crystalline | powder | 54784-011BULK INGREDIENT |
| - | LEVOLEUCOVORIN CALCIUM | powder | 54784-018BULK INGREDIENT |
Enquiry
Common questions
- Is Merck & Cie FDA approved?
- Merck & Cie holds no registered establishment of its own; 4 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Merck & Cie make?
- 4 products are listed under Merck & Cie in the openFDA NDC Directory, most often as powder. The full breakdown by dosage form and route is above. A listing count is not a sales figure.
Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.