Ibuprofen
- Product NDC
- 50844-268
- 11-digit product format
- 508440268
- Labeler code
- 50844
- Product ID
- 50844-268_c1223a96-bcbe-4dee-9246-a6a74fe9dd74
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- L.N.K. International, Inc.
- Application
- ANDA079205
- Marketing category
- ANDA
- Marketing start
- 2019-08-05
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50844-268-09 | 50844026809 | 1 BOTTLE, PLASTIC in 1 CARTON (50844-268-09) > 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2019-08-05 | 0000-00-00 | No | No | Current |