Register entry
- Registered sites
- 2
- Active NDC listings
- 26
- Labeller names
- 2
- Live patents
- 0
- Countries
- 1
- Base
- United States
Authorisation
Registered operations
Analytical testing2Finished drug manufacture2Packaging2
Sites
Registered establishments
2| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| AAA Pharmaceutical, Inc. | 681 Main Street, Lumberton, New Jersey (NJ) 08048, United States (USA) | Analytical testing, Finished drug manufacture, Packaging | 3010027650181192162 |
| AAA Pharmaceutical, Inc. | 157 W Jefferson Street, Paulsboro, New Jersey (NJ) 08066, United States (USA) | Analytical testing, Finished drug manufacture, Packaging | 2246707080164679 |
Catalogue
Drug listings by form and route
2626 active NDC listings: 26 human otc drug. By marketing category: OTC MONOGRAPH DRUG 14, ANDA 12.
| Dosage form | NDCs |
|---|---|
| tablet, coated | 15 |
| tablet | 6 |
| tablet, extended release | 3 |
| tablet, delayed release | 2 |
| Route | NDCs |
|---|---|
| oral | 26 |
| Labeller name on the listing | NDCs |
|---|---|
| aaa pharmaceutical, inc. | 21 |
| aaa pharmaceutical, inc. | 5 |
Catalogue
Marketed products
26| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| 8HR Muscle Aches and Pain | Acetaminophen | tablet, extended release, oral | 57344-201ANDA |
| Acetaminophen | Acetaminophen | tablet, coated, oral | 57344-004OTC MONOGRAPH DRUG |
| Acetaminophen PM | Acetaminophen and Diphenhydramine Hydrochloride | tablet, coated, oral | 57344-095OTC MONOGRAPH DRUG |
| Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE | tablet, coated, oral | 57344-163OTC MONOGRAPH DRUG |
| Allergy Multi Symptom | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, and PHENYLEPHRINE HYDROCHLORIDE | tablet, coated, oral | 57344-928OTC MONOGRAPH DRUG |
| Allergy Relief | Loratadine | tablet, oral | 57344-193ANDA |
| Allergy Relief | Cetirizine hydrochloride | tablet, coated, oral | 57344-194ANDA |
| Allergy Relief | Fexofenadine Hydrochloride | tablet, oral | 57344-292ANDA |
| Arthritis Pain | Acetaminophen | tablet, extended release, oral | 57344-200ANDA |
| Aspirin | ASPIRIN | tablet, coated, oral | 57344-018OTC MONOGRAPH DRUG |
| Aspirin | ASPIRIN | tablet, delayed release, oral | 57344-080OTC MONOGRAPH DRUG |
| Aspirin | ASPIRIN | tablet, delayed release, oral | 57344-146OTC MONOGRAPH DRUG |
| Diphenhydramine | DIPHENHYDRAMINE HYDROCHLORIDE | tablet, coated, oral | 57344-090OTC MONOGRAPH DRUG |
| Diphenhydramine Hydrochloride | DIPHENHYDRAMINE HYDROCHLORIDE | tablet, coated, oral | 57344-091OTC MONOGRAPH DRUG |
| IBUPROFEN | Ibuprofen | tablet, coated, oral | 57344-309ANDA |
| Ibuprofen | Ibuprofen | tablet, coated, oral | 57344-109ANDA |
| Ibuprofen | Ibuprofen | tablet, coated, oral | 57344-110ANDA |
| Ibuprofen | Ibuprofen | tablet, coated, oral | 57344-811ANDA |
| Migraine Relief | ACETAMINOPHEN, ASPIRIN and CAFFEINE | tablet, oral | 57344-205ANDA |
| Mucus Relief | Guaifenesin | tablet, extended release, oral | 57344-203ANDA |
| NAPROXEN SODIUM | NAPROXEN SODIUM | tablet, coated, oral | 57344-145ANDA |
| Pain Relief | Acetaminophen | tablet, oral | 57344-103OTC MONOGRAPH DRUG |
| Pain Relief | Acetaminophen | tablet, coated, oral | 57344-170OTC MONOGRAPH DRUG |
| Pain Relief | Acetaminophen | tablet, oral | 57344-301OTC MONOGRAPH DRUG |
| Sinus and Headache | ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE | tablet, coated, oral | 57344-923OTC MONOGRAPH DRUG |
| Stay Awake | CAFFEINE | tablet, oral | 57344-220OTC MONOGRAPH DRUG |
Compare
Comparable companies in United States
- Deseret Laboratories Incorporated2 sites · 858 NDC
- Padagis Israel Pharmaceuticals Ltd2 sites · 236 NDC
- PureTek Corporation2 sites · 178 NDC
- Cosmax Usa Corporation2 sites · 142 NDC
- Apotheca Company2 sites · 110 NDC
- Nivagen Pharmaceuticals LLC2 sites · 106 NDC
- GOJO Industries, LLC2 sites · 84 NDC
- KVK-TECH, INC.2 sites · 71 NDC
- Revlon Consumer Products Corporation2 sites · 61 NDC
- Samsung Biologics Co., Ltd.2 sites · 57 NDC
Enquiry
Common questions
- Is AAA Pharmaceutical, Inc. FDA approved?
- AAA Pharmaceutical, Inc. holds 2 FDA-registered establishments in the United States. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
- Where are AAA Pharmaceutical, Inc.'s drugs manufactured?
- The FDA register lists Lumberton, NJ; Paulsboro, NJ. Registered operations: analytical testing, finished drug manufacture, packaging.
- What drugs does AAA Pharmaceutical, Inc. make?
- 26 products are listed under AAA Pharmaceutical, Inc. in the openFDA NDC Directory, most often as tablet, coated; tablet; tablet, extended release. 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.