Ibuprofen
- Product NDC
- 11788-009
- 11-digit product format
- 117880009
- Labeler code
- 11788
- Product ID
- 11788-009_e2acadb4-d270-49d4-92cd-33db4f635fdb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- AiPing Pharmaceutical, Inc.
- Application
- ANDA202413
- Marketing category
- ANDA
- Marketing start
- 2025-12-15
- Substance
- IBUPROFEN
- Active strength
- 600 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ibuprofen
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| IBUPROFEN | 600 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | WK2XYI10QM |
| Rxcui | 197805, 197806, 197807 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
NDC, Effective, Action table| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|
| 11788-009-01 | 2026-01-20 | C162847 | 48780-1 | 1030e365-4541-111a-e063-dadaa90a10e2 | Ibuprofen Tablets, USP 300 mg, 400 mg, 600 mg and 800 mg |
| 11788-009-05 | 2026-01-20 | C162847 | 48780-1 | 1030e365-4541-111a-e063-dadaa90a10e2 | Ibuprofen Tablets, USP 300 mg, 400 mg, 600 mg and 800 mg |
| 11788-009-00 | 2024-01-30 | C162847 | 48780-1 | 1030e365-6608-111a-e063-dadaa90a10e2 | Ibuprofen Tablets, USP 400 mg, 600 mg and 800 mg |
| 11788-009-01 | 2024-01-30 | C162847 | 48780-1 | 1030e365-4541-111a-e063-dadaa90a10e2 | Ibuprofen Tablets, USP 300 mg, 400 mg, 600 mg and 800 mg |
| 11788-009-05 | 2024-01-30 | C162847 | 48780-1 | 1030e365-4541-111a-e063-dadaa90a10e2 | Ibuprofen Tablets, USP 300 mg, 400 mg, 600 mg and 800 mg |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11788-009-01 | Ibuprofen | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 20 |
| 11788-009-05 | Ibuprofen | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 20 |
| 11788-009-00 | ibuprofen | 22600 in 1 CARTON | TABLET, FILM COATED | 22600 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11788-009 | IBUPROFEN TABLET, FILM COATED [AIPING PHARMACEUTICAL INC.] | 17 | Current NDC, Legacy NDC, 2 package rows | 20220116_3e131710-2579-446e-8076-f602ecea813f.zip |
| 11788-009 | IBUPROFEN TABLET, FILM COATED [AIPING PHARMACEUTICAL, INC.] | 8 | Current NDC, Legacy NDC, 1 package rows | 20200514_3e4713d6-17cc-4296-9eb2-2edb837456a9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11788-009-00 | 11788000900 | 22600 TABLET, FILM COATED in 1 CARTON (11788-009-00) | 2016-11-23 | 0000-00-00 | No | No | Current |
| 11788-009-01 | 11788000901 | 100 TABLET, FILM COATED in 1 BOTTLE (11788-009-01) | 2025-12-15 | 0000-00-00 | No | No | Current |
| 11788-009-05 | 11788000905 | 500 TABLET, FILM COATED in 1 BOTTLE (11788-009-05) | 2025-12-15 | 0000-00-00 | No | No | Current |