Ibuprofen
- Product NDC
- 70436-182
- 11-digit product format
- 704360182
- Labeler code
- 70436
- Product ID
- 70436-182_ee2fa6b8-1588-13e1-e053-2995a90a6aa0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Slate Run Pharmaceuticals, LLC
- Application
- ANDA215318
- Marketing category
- ANDA
- Marketing start
- 2022-07-25
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 800 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 |
|---|
| 70436-182-01 | 70436018201 | 100 TABLET in 1 BOTTLE (70436-182-01) | 100 tablet | 2022-07-25 | 0000-00-00 | No | No | Current |
| 70436-182-02 | 70436018202 | 500 TABLET in 1 BOTTLE (70436-182-02) | 500 tablet | 2022-07-25 | 0000-00-00 | No | No | Current |