FDA Application
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NDC Search Results on Active Ingredient: ibuprofen
Click on Active Ingredient to view the label.
Ingredient Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
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DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 58602-887-18 | Aurohealth LLC | ANDA210676 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0363-0756-40 | Walgreens | ANDA200888 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 64380-732-11 | Strides Pharma Science Limited | ANDA200888 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 58602-887-30 | Aurohealth LLC | ANDA210676 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 69452-205-78 | Bionpharma Inc. | ANDA090397 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 64380-732-18 | Strides Pharma Science Limited | ANDA200888 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 64380-732-14 | Strides Pharma Science Limited | ANDA200888 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0363-0756-20 | Walgreens | ANDA200888 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 11673-756-40 | TARGET Corporation | ANDA200888 | HUMAN OTC DRUG | ANDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 69842-913-40 | CVS Pharmacy | ANDA210676 | HUMAN OTC DRUG | ANDA |
FAMOTIDINE; IBUPROFEN | 31722-315-90 | Camber Pharmaceuticals, Inc. | ANDA216814 | HUMAN PRESCRIPTION DRUG | ANDA |
FAMOTIDINE; IBUPROFEN | 49884-366-09 | ENDO USA, Inc. | ANDA203658 | HUMAN PRESCRIPTION DRUG | ANDA |
FAMOTIDINE; IBUPROFEN | 69306-266-30 | Doc Rx | ANDA211890 | HUMAN PRESCRIPTION DRUG | ANDA |
FAMOTIDINE; IBUPROFEN | 80425-0384-3 | Advanced Rx Pharmacy of Tennessee, LLC | ANDA216814 | HUMAN PRESCRIPTION DRUG | ANDA |
FAMOTIDINE; IBUPROFEN | 80425-0384-1 | Advanced Rx Pharmacy of Tennessee, LLC | ANDA216814 | HUMAN PRESCRIPTION DRUG | ANDA |
FAMOTIDINE; IBUPROFEN | 80425-0384-2 | Advanced Rx Pharmacy of Tennessee, LLC | ANDA216814 | HUMAN PRESCRIPTION DRUG | ANDA |
GLUCOSAMINE SULFATE; IBUPROFEN; CHONDROITIN SULFATE (BOVINE) | 61841-152-12 | Bayer HealthCare LLC. | HUMAN OTC DRUG | Export only | |
GLUCOSAMINE SULFATE; IBUPROFEN; CHONDROITIN SULFATE (BOVINE) | 61841-152-72 | Bayer HealthCare LLC. | HUMAN OTC DRUG | Export only | |
HYDROCODONE BITARTRATE; IBUPROFEN | 13107-004-99 | Aurolife Pharma, LLC | ANDA204575 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; IBUPROFEN | 67296-1655-7 | RedPharm Drug, Inc. | ANDA204575 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; IBUPROFEN | 13107-004-05 | Aurolife Pharma, LLC | ANDA204575 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; IBUPROFEN | 13107-004-11 | Aurolife Pharma, LLC | ANDA204575 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; IBUPROFEN | 13107-004-01 | Aurolife Pharma, LLC | ANDA204575 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; IBUPROFEN | 53746-116-01 | Amneal Pharmaceuticals of New York LLC | ANDA076642 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; IBUPROFEN | 61919-296-30 | DIRECT RX | ANDA077723 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCORTISONE; IBUPROFEN; POLYMYXIN B SULFATE; NEOMYCIN SULFATE; BACITRACIN ZINC | 72663-152-05 | Welly Health PBC | part348 | HUMAN OTC DRUG | OTC monograph not final |
IBUPROFEN | 51013-319-54 | PuraCap Pharmaceutical LLC | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0363-0393-37 | Walgreen Company | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 68001-435-92 | BluePoint Laboratories | ANDA209179 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-604-71 | H E B | ANDA072096 | HUMAN OTC DRUG | ANDA |
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