Motrin IB
- Product NDC
- 67751-165
- 11-digit product format
- 677510165
- Labeler code
- 67751
- Product ID
- 67751-165_6140a82d-8357-fe50-e053-2991aa0a2d7d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Navajo Manufacturing Company Inc.
- Application
- NDA019012
- Marketing category
- NDA
- Marketing start
- 2016-09-22
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67751-165-01 | 67751016501 | 1 POUCH in 1 CARTON (67751-165-01) > 2 TABLET, FILM COATED in 1 POUCH | 1 pouch | 2016-09-22 | 0000-00-00 | No | No | Current |
| 67751-165-02 | 67751016502 | 1 POUCH in 1 CARTON (67751-165-02) > 4 TABLET, FILM COATED in 1 POUCH | 1 pouch | 2016-09-22 | 0000-00-00 | No | No | Current |