Ibuprofen PM
- Product NDC
- 69842-656
- 11-digit product format
- 698420656
- Labeler code
- 69842
- Product ID
- 69842-656_a4876887-b6b9-4582-a51e-7b009939b832
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN, DIPHENHYDRAMINE HCL
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- CVS Pharmacy
- Application
- ANDA200888
- Marketing category
- ANDA
- Marketing start
- 2019-03-31
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69842-656-40 | 69842065640 | 1 BOTTLE, PLASTIC in 1 BOX (69842-656-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2019-03-31 | 0000-00-00 | No | No | Current |