Ibuprofen
- Product NDC
- 41163-212
- 11-digit product format
- 411630212
- Labeler code
- 41163
- Product ID
- 41163-212_80c77976-91f7-3f54-e053-2a91aa0a79b0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- SUPERVALU INC.
- Application
- ANDA091355
- Marketing category
- ANDA
- Marketing start
- 2019-01-31
- 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 |
|---|
| 41163-212-02 | 41163021202 | 1 BOTTLE, PLASTIC in 1 CARTON (41163-212-02) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC | 2019-01-31 | 0000-00-00 | No | No | Current |
| 41163-212-03 | 41163021203 | 1 BOTTLE, PLASTIC in 1 CARTON (41163-212-03) > 100 TABLET, COATED in 1 BOTTLE, PLASTIC | 2019-01-31 | 0000-00-00 | No | No | Current |
| 41163-212-05 | 41163021205 | 500 TABLET, COATED in 1 BOTTLE, PLASTIC (41163-212-05) | 2019-01-31 | 0000-00-00 | No | No | Current |