Ibuprofen
- Product NDC
- 11673-197
- 11-digit product format
- 116730197
- Labeler code
- 11673
- Product ID
- 11673-197_68ebcdcb-3f3c-47ca-bd2c-505f7726f0a7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- TARGET Corporation
- Application
- ANDA078682
- Marketing category
- ANDA
- Marketing start
- 2010-08-01
- Marketing end
- 2021-12-31
- 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 |
|---|
| 11673-197-03 | 11673019703 | 300 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (11673-197-03) | 2010-08-01 | 2021-12-31 | No | No | Current |
| 11673-197-16 | 11673019716 | 1 BOTTLE, PLASTIC in 1 BOX (11673-197-16) > 160 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2010-08-01 | 2021-12-31 | No | No | Current |
| 11673-197-40 | 11673019740 | 1 BOTTLE, PLASTIC in 1 BOX (11673-197-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2010-08-01 | 2021-12-31 | No | No | Current |
| 11673-197-80 | 11673019780 | 1 BOTTLE, PLASTIC in 1 BOX (11673-197-80) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2010-08-01 | 2021-12-31 | No | No | Current |