sunmark ibuprofen is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Ibuprofen.
| Product ID | 71335-0746_406b71d8-df46-4be6-8d2e-dc77d0cda262 |
| NDC | 71335-0746 |
| Product Type | Human Otc Drug |
| Proprietary Name | sunmark ibuprofen |
| Generic Name | Ibuprofen |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2003-06-24 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA072096 |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | IBUPROFEN |
| Active Ingredient Strength | 200 mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 2016-05-12 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA072096 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-05-12 |
| Marketing Category | ANDA |
| Application Number | ANDA072096 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-05-12 |
| Marketing Category | ANDA |
| Application Number | ANDA072096 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-05-12 |
| Marketing Category | ANDA |
| Application Number | ANDA072096 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-05-12 |
| Marketing Category | ANDA |
| Application Number | ANDA072096 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-05-12 |
| Marketing Category | ANDA |
| Application Number | ANDA072096 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-05-12 |
| Marketing Category | ANDA |
| Application Number | ANDA072096 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-05-12 |
| Marketing Category | ANDA |
| Application Number | ANDA072096 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-05-12 |
| Marketing Category | ANDA |
| Application Number | ANDA072096 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-05-12 |
| Marketing Category | ANDA |
| Application Number | ANDA072096 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-05-12 |
| Ingredient | Strength |
|---|---|
| IBUPROFEN | 200 mg/1 |
| SPL SET ID: | 498a9f93-1700-4199-991b-2fe05a15143f |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| PHarm Class EPC | |
| NUI Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 71335-0746 | sunmark ibuprofen | sunmark ibuprofen |
| 49348-196 | sunmark ibuprofen | sunmark ibuprofen |
| 49348-642 | sunmark ibuprofen | sunmark ibuprofen |
| 49348-229 | sunmark ibuprofen | sunmark ibuprofen |
| 49348-706 | sunmark ibuprofen | sunmark ibuprofen |
| 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 |