NDC 63629-8851

Ibuprofen Oral

Ibuprofen Oral

Ibuprofen Oral is a Oral Suspension in the Human Otc Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Ibuprofen.

Product ID63629-8851_853dd713-aa5a-47d6-8821-46a92b53e21d
NDC63629-8851
Product TypeHuman Otc Drug
Proprietary NameIbuprofen Oral
Generic NameIbuprofen Oral
Dosage FormSuspension
Route of AdministrationORAL
Marketing Start Date2019-09-18
Marketing CategoryANDA /
Application NumberANDA210602
Labeler NameBryant Ranch Prepack
Substance NameIBUPROFEN
Active Ingredient Strength100 mg/5mL
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 63629-8851-1

1 BOTTLE in 1 CARTON (63629-8851-1) > 118 mL in 1 BOTTLE
Marketing Start Date2021-09-20
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Ibuprofen Oral" or generic name "Ibuprofen Oral"

NDCBrand NameGeneric Name
50090-4129Ibuprofen OralIbuprofen Oral
63629-1230Ibuprofen OralIbuprofen Oral
63629-8540Ibuprofen OralIbuprofen Oral
63629-8851Ibuprofen OralIbuprofen Oral
63629-8852Ibuprofen OralIbuprofen Oral
63629-8853Ibuprofen OralIbuprofen Oral
68071-1628Ibuprofen OralIbuprofen Oral
68788-7984Ibuprofen OralIbuprofen Oral
69230-308Ibuprofen OralIbuprofen Oral
69230-309Ibuprofen OralIbuprofen Oral
69230-310Ibuprofen OralIbuprofen Oral
69230-311Ibuprofen OralIbuprofen Oral
70677-0150Ibuprofen OralIbuprofen Oral
70677-0151Ibuprofen OralIbuprofen Oral
70677-0152Ibuprofen OralIbuprofen Oral
70677-0153Ibuprofen OralIbuprofen Oral
59651-032IbuprofenIbuprofen Oral

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.