IBUPROFEN
- Product NDC
- 68210-4141
- 11-digit product format
- 682104141
- Labeler code
- 68210
- Product ID
- 68210-4141_ee8e73f9-3140-ab4a-e053-2a95a90aa4c6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- SPIRIT PHARMACEUTICALS,LLC
- Application
- ANDA079205
- Marketing category
- ANDA
- Marketing start
- 2021-04-28
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68210-4141-6 | 68210414106 | 1 BOTTLE in 1 PACKAGE (68210-4141-6) > 6 CAPSULE, LIQUID FILLED in 1 BOTTLE | 1 bottle | 2021-04-28 | 0000-00-00 | No | No | Current |