Ibuprofen IB
- Product NDC
- 67091-130
- 11-digit product format
- 670910130
- Labeler code
- 67091
- Product ID
- 67091-130_94554744-2e7c-e2fa-e053-2a95a90ac1f7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- WinCo Foods, LLC
- Application
- ANDA091355
- Marketing category
- ANDA
- Marketing start
- 2014-12-15
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 67091-130-10 | 67091013010 | 1 BOTTLE, PLASTIC in 1 CARTON (67091-130-10) > 100 TABLET, COATED in 1 BOTTLE, PLASTIC | 2014-12-15 | 0000-00-00 | No | No | Current |
| 67091-130-50 | 67091013050 | 1 BOTTLE, PLASTIC in 1 CARTON (67091-130-50) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC | 2014-12-15 | 0000-00-00 | No | No | Current |