Ibuprofen
- Product NDC
- 41163-392
- 11-digit product format
- 411630392
- Labeler code
- 41163
- Product ID
- 41163-392_e12b3a61-be40-429c-b2d9-233cb2ac2b80
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- SUPERVALU INC.
- Application
- ANDA075139
- Marketing category
- ANDA
- Marketing start
- 1999-03-01
- Marketing end
- 2023-01-07
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41163-392-12 | 41163039212 | 1 BOTTLE in 1 CARTON (41163-392-12) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 1999-03-01 | 2023-01-07 | No | No | Current |
| 41163-392-15 | 41163039215 | 1 BOTTLE in 1 CARTON (41163-392-15) > 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 1999-03-01 | 2021-03-19 | No | No | Current |