NDC 50580-110
Motrin IB
Ibuprofen
Motrin IB is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Johnson & Johnson Consumer Inc., Mcneil Consumer Healthcare Division. The primary component is Ibuprofen.
| Product ID | 50580-110_4e10c377-3895-4550-b6a4-9cb03805dcb2 |
| NDC | 50580-110 |
| Product Type | Human Otc Drug |
| Proprietary Name | Motrin IB |
| Generic Name | Ibuprofen |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2000-08-01 |
| Marketing Category | NDA / NDA |
| Application Number | NDA019012 |
| Labeler Name | Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
| Substance Name | IBUPROFEN |
| Active Ingredient Strength | 200 mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
Packaging
NDC 50580-110-52
50 POUCH in 1 TRAY (50580-110-52) > 2 TABLET, FILM COATED in 1 POUCH (50580-110-19)
| Marketing Start Date | 2000-08-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 50580-110-75 [50580011075]
Motrin IB TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA019012 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2000-08-01 |
| Marketing End Date | 2013-10-25 |
NDC 50580-110-62 [50580011062]
Motrin IB TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA019012 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2000-08-01 |
| Marketing End Date | 2017-06-23 |
NDC 50580-110-60 [50580011060]
Motrin IB TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA019012 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2000-08-01 |
| Marketing End Date | 2019-01-01 |
NDC 50580-110-76 [50580011076]
Motrin IB TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA019012 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2000-08-01 |
| Marketing End Date | 2013-10-25 |
NDC 50580-110-38 [50580011038]
Motrin IB TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA019012 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2000-08-01 |
| Marketing End Date | 2017-06-23 |
NDC 50580-110-37 [50580011037]
Motrin IB TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA019012 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2000-08-01 |
| Marketing End Date | 2015-09-08 |
NDC 50580-110-10 [50580011010]
Motrin IB TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA019012 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2000-08-01 |
| Marketing End Date | 2017-06-23 |
NDC 50580-110-64 [50580011064]
Motrin IB TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA019012 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2000-08-01 |
| Marketing End Date | 2015-09-08 |
NDC 50580-110-95 [50580011095]
Motrin IB TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA019012 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2000-08-01 |
| Marketing End Date | 2013-10-25 |
NDC 50580-110-01 [50580011001]
Motrin IB TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA019012 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2000-08-01 |
| Marketing End Date | 2015-04-05 |
NDC 50580-110-09 [50580011009]
Motrin IB TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA019012 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2000-08-01 |
| Marketing End Date | 2013-04-30 |
NDC 50580-110-19 [50580011019]
Motrin IB TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA019012 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2000-08-01 |
| Marketing End Date | 2019-11-30 |
NDC 50580-110-02 [50580011002]
Motrin IB TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA019012 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2000-08-01 |
| Marketing End Date | 2017-06-23 |
NDC 50580-110-03 [50580011003]
Motrin IB TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA019012 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2000-08-01 |
| Marketing End Date | 2015-09-08 |
NDC 50580-110-07 [50580011007]
Motrin IB TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA019012 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2013-04-16 |
| Marketing End Date | 2017-06-23 |
NDC 50580-110-51 [50580011051]
Motrin IB TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA019012 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2000-08-01 |
| Marketing End Date | 2018-12-31 |
NDC 50580-110-52 [50580011052]
Motrin IB TABLET, FILM COATED
| Marketing Category | NDA |
| Application Number | NDA019012 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2000-08-01 |
| Marketing End Date | 2019-11-30 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| IBUPROFEN | 200 mg/1 |
OpenFDA Data
| SPL SET ID: | 5bca517f-94a5-428c-b716-80c6b0b86980 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| PHarm Class EPC | |
| NUI Code |
NDC Crossover Matching brand name "Motrin IB" or generic name "Ibuprofen"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 67751-165 | Motrin IB | Motrin IB |
| 29485-1465 | Motrin IB | Motrin IB |
| 50269-000 | MOTRIN IB | MOTRIN IB |
| 50580-230 | Motrin IB | Motrin IB |
| 50580-409 | Motrin IB | Motrin IB |
| 50580-110 | Motrin IB | Motrin IB |
| 66715-9812 | Motrin IB | Motrin IB |
| 66715-9712 | Motrin IB | Motrin IB |
| 67414-240 | Motrin IB | Motrin IB |
| 73097-008 | Motrin IB | Motrin IB |
| 0113-1461 | basic care childrens ibuprofen | Ibuprofen |
| 0113-7619 | basic care childrens ibuprofen | ibuprofen |
| 0113-7660 | basic care childrens ibuprofen | Ibuprofen |
| 0113-7897 | Basic Care childrens ibuprofen | Ibuprofen |
| 0113-0788 | Basic Care ibuprofen | Ibuprofen |
| 0113-7131 | basic care ibuprofen | Ibuprofen |
| 0113-7517 | basic care ibuprofen | Ibuprofen |
| 0113-7604 | Basic Care Ibuprofen | Ibuprofen |
| 0121-0917 | Childrens Ibuprofen | Ibuprofen |
| 0121-0914 | Childrens Ibuprofen Oral Suspension | Ibuprofen |
| 0113-2461 | Good Sense Childrens Ibuprofen | Ibuprofen |
| 0113-0057 | Good Sense ibuprofen | ibuprofen |
| 0113-0074 | Good Sense ibuprofen | Ibuprofen |
| 0113-0166 | good sense ibuprofen | Ibuprofen |
| 0113-0298 | good sense ibuprofen | Ibuprofen |
| 0113-0461 | Good Sense ibuprofen | Ibuprofen |
| 0113-0517 | Good Sense ibuprofen | Ibuprofen |
| 0113-0604 | good sense ibuprofen | Ibuprofen |
| 0113-0647 | good sense ibuprofen | Ibuprofen |
| 0113-0660 | Good Sense Ibuprofen | Ibuprofen |
| 0113-0685 | Good Sense Ibuprofen | Ibuprofen |
| 0113-0897 | good sense ibuprofen | Ibuprofen |
| 0113-1212 | Good Sense Ibuprofen | Ibuprofen |
| 0113-4501 | good sense ibuprofen | ibuprofen |
| 0113-0040 | Good Sense Infants Ibuprofen | Ibuprofen |
Trademark Results [Motrin IB]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MOTRIN IB 75433948 2371520 Dead/Cancelled |
JOHNSON & JOHNSON 1998-02-13 |
 MOTRIN IB 75433872 2390239 Dead/Cancelled |
JOHNSON & JOHNSON 1998-02-13 |
 MOTRIN IB 75433860 2371519 Dead/Cancelled |
JOHNSON & JOHNSON 1998-02-13 |
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