Register entryRepackager / relabeller
- Registered sites
- 1
- Active NDC listings
- 9
- Live patents
- 0
- Countries
- 1
- Base
- United States
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Morning Star OTC | 145 S Anderson St, Los Angeles, California (CA) 90033, United States (USA) | Repackaging | 3008674424078589357 |
Catalogue
Drug listings by form and route
99 active NDC listings: 9 human otc drug. By marketing category: OTC MONOGRAPH DRUG 6, NDA 2, ANDA 1.
| Dosage form | NDCs |
|---|---|
| tablet, film coated | 6 |
| solution/ drops | 1 |
| tablet, chewable | 1 |
| tablet, coated | 1 |
| Route | NDCs |
|---|---|
| oral | 8 |
| ophthalmic | 1 |
| Labeller name on the listing | NDCs |
|---|---|
| morning star otc | 9 |
Catalogue
Marketed products
9| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Benadryl | Diphenhydramine Hydrochloride | tablet, film coated, oral | 53209-3001OTC MONOGRAPH DRUG |
| Motrin IB | Ibuprofen | tablet, film coated, oral | 53209-2001ANDA |
| Pepcid Complete | Famotidine, Calcium carbonate, and Magnesium hydroxide | tablet, chewable, oral | 53209-4001NDA |
| TYLENOL Cold Plus Flu Severe | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride | tablet, film coated, oral | 53209-1003OTC MONOGRAPH DRUG |
| TYLENOL Extra Strength | Acetaminophen | tablet, film coated, oral | 53209-1001OTC MONOGRAPH DRUG |
| Tylenol PM Extra Strength | acetaminophen and diphenhydramine hydrochloride | tablet, film coated, oral | 53209-1002OTC MONOGRAPH DRUG |
| Tylenol Sinus Severe | Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride | tablet, coated, oral | 53209-1004OTC MONOGRAPH DRUG |
| Visine Red Eye Hydrating Comfort Eye Drops | TETRAHYDROZOLINE HYDROCHLORIDE and Polyethylene Glycol 400 | solution/ drops, ophthalmic | 53209-6001OTC MONOGRAPH DRUG |
| Zyrtec Allergy | Cetirizine Hydrochloride | tablet, film coated, oral | 53209-5001NDA |
Neighbours
Registered in the same town
10- Baxalta US Inc.LOS ANGELES, CA
- Pharmalogic Holdings Corp.Los Angeles, CA
- Sotera Health LLCLos Angeles, CA
- Grifols Therapeutics LLCLos Angeles, CA
- Calox IncLos Angeles, CA
- Alexso, IncLos Angeles, CA
- Hyland's Consumer Health IncLos Angeles, CA
- MADISON ONE ACME INCLOS ANGELES, CA
- XSEER PHARMACEUTICALS INC.Los Angeles, CA
- YES SALES INCLos Angeles, CA
Compare
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- Camber Pharmaceuticals, Inc.1 site · 640 NDC
- Northwind Health Company, LLC1 site · 580 NDC
- Direct Rx1 site · 554 NDC
- Professional Compounding Centers of America dba PCCA1 site · 487 NDC
- Coupler LLC1 site · 469 NDC
Enquiry
Common questions
- Is Morning Star OTC FDA approved?
- Morning Star OTC holds 1 FDA-registered establishment 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 Morning Star OTC's registered sites?
- The FDA register lists Los Angeles, CA. Registered operations: repackaging.
- What drugs does Morning Star OTC make?
- 9 products are listed under Morning Star OTC in the openFDA NDC Directory, most often as tablet, film coated; solution/ drops; tablet, chewable. 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.