Register entry
- Registered sites
- 0
- Active NDC listings
- 9
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
99 active NDC listings: 9 human otc drug. By marketing category: OTC MONOGRAPH DRUG 7, ANDA 2.
| Dosage form | NDCs |
|---|---|
| tablet | 4 |
| capsule | 2 |
| liquid | 2 |
| syrup | 1 |
| Route | NDCs |
|---|---|
| oral | 9 |
| Labeller name on the listing | NDCs |
|---|---|
| sda laboratories, inc. | 9 |
Catalogue
Marketed products
9| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Anti-Diarrheal | Loperamide Hydrochloride | tablet, oral | 66424-725ANDA |
| CETIRIZINE HYDROCHLORIDE 10 MG | CETIRIZINE HYDROCHLORIDE | tablet, oral | 66424-564ANDA |
| Diphenhydramine HCL | Diphenhydramine HCL | capsule, oral | 66424-020OTC MONOGRAPH DRUG |
| Diphenhydramine HCL | Diphenhydramine HCL | capsule, oral | 66424-021OTC MONOGRAPH DRUG |
| MUCUS RELIEF | Guaifenesin | tablet, oral | 66424-001OTC MONOGRAPH DRUG |
| SDA Laboratories Tussin | Guaifenesin | liquid, oral | 66424-563OTC MONOGRAPH DRUG |
| SDA Laboratories Tussin DM | Dextromethorphan HBr, Guaifenesin | liquid, oral | 66424-565OTC MONOGRAPH DRUG |
| SENNA Syrup | Sennosides A and B | syrup, oral | 66424-562OTC MONOGRAPH DRUG |
| Stimulant Laxative Enteric Coated | Bisacodyl | tablet, oral | 66424-002OTC MONOGRAPH DRUG |
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Enquiry
Common questions
- Is SDA Laboratories, Inc. FDA approved?
- SDA Laboratories, Inc. holds no registered establishment of its own; 9 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does SDA Laboratories, Inc. make?
- 9 products are listed under SDA Laboratories, Inc. in the openFDA NDC Directory, most often as tablet; capsule; liquid. 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.