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NDC 00573-0150-32 ADVIL 200 mg/1 Details
ADVIL 200 mg/1
ADVIL is a ORAL TABLET, COATED in the HUMAN OTC DRUG category. It is labeled and distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. The primary component is IBUPROFEN.
Product Information
| NDC | 00573-0150 |
|---|---|
| Product ID | 0573-0150_50ff83c8-c41f-4a9c-adb1-cb060bf21bc3 |
| Associated GPIs | 66100020000305 |
| GCN Sequence Number | 008346 |
| GCN Sequence Number Description | ibuprofen TABLET 200 MG ORAL |
| HIC3 | S2B |
| HIC3 Description | NSAIDS, CYCLOOXYGENASE INHIBITOR TYPE ANALGESICS |
| GCN | 35743 |
| HICL Sequence Number | 003723 |
| HICL Sequence Number Description | IBUPROFEN |
| Brand/Generic | Brand |
| Proprietary Name | ADVIL |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | ibuprofen |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, COATED |
| Route | ORAL |
| Active Ingredient Strength | 200 |
| Active Ingredient Units | mg/1 |
| Substance Name | IBUPROFEN |
| Labeler Name | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
| Pharmaceutical Class | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA018989 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00573-0150-32 (00573015032)
| NDC Package Code | 0573-0150-32 |
|---|---|
| Billing NDC | 00573015032 |
| Package | 1 BOTTLE in 1 CARTON (0573-0150-32) / 60 TABLET, COATED in 1 BOTTLE |
| Marketing Start Date | 1984-05-18 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |