rexall ibuprofen
- Product NDC
- 55910-517
- 11-digit product format
- 559100517
- Labeler code
- 55910
- Product ID
- 55910-517_3a735b15-2cf1-47f9-a684-0a4804d04258
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Dolgencorp, LLC
- Application
- ANDA077349
- Marketing category
- ANDA
- Marketing start
- 2012-09-06
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 55910-517-71 | 55910051771 | 1 BOTTLE in 1 CARTON (55910-517-71) > 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2012-09-06 | 0000-00-00 | No | No | Current |