Ibuprofen
- Product NDC
- 41250-801
- 11-digit product format
- 412500801
- Labeler code
- 41250
- Product ID
- 41250-801_ae419268-b2f9-4693-8b1d-f43201a00df4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Meijer, Inc.
- Application
- ANDA072096
- Marketing category
- ANDA
- Marketing start
- 2017-07-12
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41250-801-78 | 41250080178 | 100 TABLET, FILM COATED in 1 BOTTLE (41250-801-78) | | 2017-07-12 | 0000-00-00 | No | No | Current |
| 41250-801-82 | 41250080182 | 2 BOTTLE in 1 CARTON (41250-801-82) > 100 TABLET, FILM COATED in 1 BOTTLE | 2 bottle | 2017-07-12 | 0000-00-00 | No | No | Current |