IBUPROFEN
- Product NDC
- 62011-0016
- 11-digit product format
- 620110016
- Labeler code
- 62011
- Product ID
- 62011-0016_8dbaf09d-4bde-41f1-bce9-d7f8c01b132a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA078682
- Marketing category
- ANDA
- Marketing start
- 2012-04-09
- Marketing end
- 2024-04-26
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62011-0016-1 | 62011001601 | 1 BOTTLE in 1 BOX (62011-0016-1) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE | 1 bottle | 2012-04-09 | 0000-00-00 | No | No | Current |