Register entry
- Registered sites
- 0
- Active NDC listings
- 19
- Labeller names
- 3
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
1919 active NDC listings: 19 human otc drug. By marketing category: OTC MONOGRAPH DRUG 10, ANDA 9.
| Dosage form | NDCs |
|---|---|
| tablet, coated | 8 |
| liquid | 2 |
| tablet | 2 |
| tablet, extended release | 2 |
| capsule, liquid filled | 1 |
| soap | 1 |
| solution | 1 |
| tablet, chewable | 1 |
| tablet, delayed release | 1 |
| Route | NDCs |
|---|---|
| oral | 15 |
| topical | 4 |
| Labeller name on the listing | NDCs |
|---|---|
| amerifoods trading company | 14 |
| amerifoods trading company | 3 |
| amerifoods trading co | 2 |
Catalogue
Marketed products
19| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| ASPIRIN | ASPIRIN | tablet, delayed release, oral | 61504-080OTC MONOGRAPH DRUG |
| Acetaminophen | Acetaminophen | tablet, coated, oral | 61504-104OTC MONOGRAPH DRUG |
| Allergy Relief | DIPHENHYDRAMINE HYDROCHLORIDE | tablet, coated, oral | 61504-090OTC MONOGRAPH DRUG |
| Allergy Relief | Fexofenadine Hydrochloride | tablet, oral | 61504-192ANDA |
| Allergy Relief | Loratadine | tablet, oral | 61504-193ANDA |
| Allergy Relief | Cetirizine hydrochloride | tablet, coated, oral | 61504-194ANDA |
| Arthritis Pain | Acetaminophen | tablet, extended release, oral | 61504-200ANDA |
| First Street Antibacterial Liquid Hand | Benzalkonium Chloride | liquid, topical | 61504-551OTC MONOGRAPH DRUG |
| First Street Dishwashing Concentrate and Antibacterial Hand | Benzalkonium Chloride | soap, topical | 61504-552OTC MONOGRAPH DRUG |
| Hydrogen Peroxide | HYDROGEN PEROXIDE | solution, topical | 61504-871OTC MONOGRAPH DRUG |
| IBUPROFEN | Ibuprofen | tablet, coated, oral | 61504-110ANDA |
| IRIS | ISOPROPYL ALCOHOL | liquid, topical | 61504-810OTC MONOGRAPH DRUG |
| Ibuprofen | Ibuprofen | tablet, coated, oral | 61504-109ANDA |
| Ibuprofen | Ibuprofen | capsule, liquid filled, oral | 61504-185ANDA |
| Low Dose Aspiriun | ASPIRIN | tablet, chewable, oral | 61504-105OTC MONOGRAPH DRUG |
| Mucus Relief | Guaifenesin | tablet, extended release, oral | 61504-204ANDA |
| Naproxen Sodium | NAPROXEN SODIUM | tablet, coated, oral | 61504-145ANDA |
| Nighttime SleepAid | DIPHENHYDRAMINE HYDROCHLORIDE | tablet, coated, oral | 61504-091OTC MONOGRAPH DRUG |
| Pain Relief PM | Acetaminophen and Diphenhydramine Hydrochloride | tablet, coated, oral | 61504-095OTC MONOGRAPH DRUG |
Compare
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Enquiry
Common questions
- Is Amerifoods Trading Company FDA approved?
- Amerifoods Trading Company holds no registered establishment of its own; 19 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Amerifoods Trading Company make?
- 19 products are listed under Amerifoods Trading Company in the openFDA NDC Directory, most often as tablet, coated; liquid; tablet. 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.