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NDC 71205-0604-60 IBU 400 mg/1 Details
IBU 400 mg/1
IBU is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is IBUPROFEN.
Product Information
| NDC | 71205-0604 |
|---|---|
| Product ID | 71205-604_f49b4e82-120c-4012-b4b3-78c0f89ae8fd |
| Associated GPIs | 66100020000320 |
| GCN Sequence Number | 008348 |
| GCN Sequence Number Description | ibuprofen TABLET 400 MG ORAL |
| HIC3 | S2B |
| HIC3 Description | NSAIDS, CYCLOOXYGENASE INHIBITOR TYPE ANALGESICS |
| GCN | 35741 |
| HICL Sequence Number | 003723 |
| HICL Sequence Number Description | IBUPROFEN |
| Brand/Generic | Generic |
| Proprietary Name | IBU |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Ibuprofen |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 400 |
| Active Ingredient Units | mg/1 |
| Substance Name | IBUPROFEN |
| Labeler Name | Proficient Rx LP |
| Pharmaceutical Class | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA075682 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 71205-0604-60 (71205060460)
| NDC Package Code | 71205-604-60 |
|---|---|
| Billing NDC | 71205060460 |
| Package | 60 TABLET in 1 BOTTLE (71205-604-60) |
| Marketing Start Date | 2021-08-27 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |