Ibuprofen
- Product NDC
- 11673-749
- 11-digit product format
- 116730749
- Labeler code
- 11673
- Product ID
- 11673-749_301c51dc-c546-46bc-828b-0fb99ab1b53f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- TARGET Corporation
- Application
- ANDA206568
- Marketing category
- ANDA
- Marketing start
- 2018-01-31
- Marketing end
- 2025-05-30
- Substance
- IBUPROFEN
- Active strength
- 200 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-749 | IBUPROFEN CAPSULE, LIQUID FILLED [TARGET CORPORATION] | 3 | Legacy NDC | 20221118_a45296d4-af8b-423a-8154-cc7c99b2a9cb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-749-12 | 11673074912 | 120 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (11673-749-12) | 2018-01-31 | 2025-05-30 | No | No | Current |