Drug company (FDA labeler)
AiPing Pharmaceutical, Inc.
NDC labeler code: 11788
What is a labeler?
The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.
Official FDA data only
Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.
Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.
Prescription medicines
- Haloperidol6 products
- Amitriptyline hydrochloride6 products
- BuspironeBucapsol · 5 products
- GlipizideGlucotrol XL · 5 products
- Sotalol hydrochlorideBetapace, Sotalol Hydrochloride Af, Betapace Af · 4 products
- MeloxicamZybic, Xifyrm, Qamzova · 4 products
- CelecoxibCelebrex, Vyscoxa, Elyxyb - Celecoxib · 4 products
- RosuvastatinCrestor · 4 products
- Captopril4 products
- IbuprofenIbu, Caldolor · 3 products
- Losartan potassiumLosortan Potassium, Cozaar, Arbli · 3 products
- Cyclobenzaprine hydrochlorideAmrix, Tonmya, Fexmid · 3 products
- Metformin hydrochlorideGlumetza · 2 products
- TicagrelorBrilinta · 2 products
- AzithromycinZithromax, Azasite · 2 products
- Methimazole2 products
- DoxycyclineDoxy 100, Acticlate Cap, Doryx Mpc · 1 product
- Sevelamer carbonateRenvela · 1 product
- CholestyramineQuestran, Prevalite, Cholestyramine Light · 1 product
FDA applications for these products
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| March 24, 2026 | ANDA219006 | Ticagrelor TICAGRELOR | Zhejiang Jingxin |
| October 1, 2025 | ANDA219978 | Doxycycline DOXYCYCLINE | Aiping Pharm Inc |
| October 24, 2024 | ANDA215998 | Sevelamer carbonate SEVELAMER CARBONATE | Shandong Xinhua |
| July 27, 2023 | ANDA217036 | Azithromycin AZITHROMYCIN | Zhejiang Poly Pharm |
| January 27, 2023 | ANDA214442 | Captopril CAPTOPRIL | Aiping Pharm Inc |
| January 21, 2022 | ANDA214877 | Cholestyramine CHOLESTYRAMINE | Aiping Pharm Inc |
| April 7, 2020 | ANDA212654 | Amitriptyline hydrochloride AMITRIPTYLINE HYDROCHLORIDE | Aiping Pharm Inc |
| August 7, 2019 | ANDA208856 | Celecoxib CELECOXIB | Qingdao Baheal Pharm |
| March 1, 2019 | ANDA206513 | Rosuvastatin ROSUVASTATIN CALCIUM | Zhejiang Jingxin |
| December 27, 2018 | ANDA209993 | Metformin hydrochloride METFORMIN HYDROCHLORIDE | Qingdao Baheal Pharm |
| November 23, 2016 | ANDA202413 | Ibuprofen IBUPROFEN | Shandong Xinhua |
| December 16, 2015 | ANDA202087 | Buspirone BUSPIRONE HYDROCHLORIDE | Aiping Pharm Inc |
| October 6, 2010 | ANDA090544 | Losartan potassium LOSARTAN POTASSIUM | Aiping Pharm Inc |
| July 19, 2006 | ANDA077920 | Meloxicam MELOXICAM | Aiping Pharm Inc |
| February 18, 2005 | ANDA040547 | Methimazole METHIMAZOLE | Aiping Pharm Inc |
| April 27, 2001 | ANDA075500 | Sotalol hydrochloride SORINE | Aiping Pharm Inc |
| April 7, 1995 | ANDA074305 | Glipizide GLIPIZIDE | Aiping Pharm Inc |
| November 19, 1991 | ANDA072854 | Cyclobenzaprine hydrochloride CYCLOBENZAPRINE HYDROCHLORIDE | Aiping Pharm Inc |
| February 17, 1987 | ANDA071130 | Haloperidol HALOPERIDOL | Aiping Pharm Inc |
The sponsor is the company that holds the FDA application; it can differ from the labeler.
Recall timeline
No recall of these products (by NDC code) appears in the FDA enforcement reports.
Next steps
- Find a pharmacy near youAsk which company made your medicine and whether it is recalled
- Latest FDA drug recallsAll companies, newest first
- All drug companiesA to Z
- All prescription drugs A to ZSearch by generic, brand or Spanish name
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026