Ibuprofen PM
- Product NDC
- 11673-756
- 11-digit product format
- 116730756
- Labeler code
- 11673
- Product ID
- 11673-756_895f988d-e624-440a-8863-9c4e060fa15b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN, DIPHENHYDRAMINE HCL
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- TARGET Corporation
- Application
- ANDA200888
- Marketing category
- ANDA
- Marketing start
- 2018-03-31
- Marketing end
- 2025-03-31
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN
- Active strength
- 25 mg/1; mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], 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 |
|---|
| 11673-756-40 | 11673075640 | 1 BOTTLE, PLASTIC in 1 BOX (11673-756-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2018-03-31 | 0000-00-00 | No | No | Current |