Ibuprofen
- Product NDC
- 0536-3603
- 11-digit product format
- 005363603
- Labeler code
- 0536
- Product ID
- 0536-3603_8f2e94ba-b4a9-4b0d-b35e-e40e73451222
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Rugby Laboratories, Inc.
- Application
- ANDA078682
- Marketing category
- ANDA
- Marketing start
- 2012-03-26
- Marketing end
- 2021-12-30
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- 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 |
|---|
| 0536-3603-30 | 00536360330 | 80 CAPSULE, LIQUID FILLED in 1 BOTTLE (0536-3603-30) | 2012-03-26 | 2021-12-30 | No | No | Current |