Ibuprofen
- Product NDC
- 0363-0749
- 11-digit product format
- 003630749
- Labeler code
- 0363
- Product ID
- 0363-0749_1c50d1e4-dfe2-406c-b9ad-e69eb65bf093
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Walgreens
- Application
- ANDA206568
- Marketing category
- ANDA
- Marketing start
- 2018-01-31
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- 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 |
|---|
| 0363-0749 | IBUPROFEN CAPSULE, LIQUID FILLED [WALGREENS] | 4 | Legacy NDC | 20250508_cb901e03-3341-4fbb-9fd2-555bfa543ed5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0363-0749-12 | 00363074912 | 120 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (0363-0749-12) | 2018-01-31 | 0000-00-00 | No | No | Current |