Ibuprofen
- Product NDC
- 43063-013
- 11-digit product format
- 430630013
- Labeler code
- 43063
- Product ID
- 43063-013_c831cfc8-c143-9da1-e053-2a95a90ad23b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA078558
- Marketing category
- ANDA
- Marketing start
- 2009-11-23
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 800 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 43063-013-04 | 43063001304 | 4 TABLET in 1 BOTTLE, PLASTIC (43063-013-04) | 4 tablet | 2013-02-20 | 0000-00-00 | No | No | Current |
| 43063-013-06 | 43063001306 | 6 TABLET in 1 BOTTLE, PLASTIC (43063-013-06) | 6 tablet | 2013-02-20 | 0000-00-00 | No | No | Current |