Ibuprofen
- Product NDC
- 49738-112
- 11-digit product format
- 497380112
- Labeler code
- 49738
- Product ID
- 49738-112_946b59b1-5c0c-bb67-e053-2a95a90aab2f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- SMART SENSE (KMART)
- Application
- ANDA091355
- Marketing category
- ANDA
- Marketing start
- 2017-07-27
- 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 |
|---|
| 49738-112-02 | 49738011202 | 1 BOTTLE, PLASTIC in 1 CARTON (49738-112-02) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC | 2017-07-27 | 0000-00-00 | No | No | Current |