Ibuprofen
- Product NDC
- 55910-651
- 11-digit product format
- 559100651
- Labeler code
- 55910
- Product ID
- 55910-651_8352756a-7703-4f25-980c-1087d8c8223b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)
- Application
- ANDA206999
- Marketing category
- ANDA
- Marketing start
- 2018-09-30
- Marketing end
- 2025-01-31
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55910-651-40 | 55910065140 | 1 BOTTLE, PLASTIC in 1 BOX (55910-651-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2018-09-30 | 0000-00-00 | No | No | Current |