ibuprofen
- Product NDC
- 0363-0705
- 11-digit product format
- 003630705
- Labeler code
- 0363
- Product ID
- 0363-0705_31e831aa-0dc1-4e45-9444-6d3fb44f4887
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Walgreen Company
- Application
- ANDA072096
- Marketing category
- ANDA
- Marketing start
- 2021-10-31
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-0705 | IBUPROFEN TABLET, FILM COATED [WALGREEN COMPANY] | 3 | Legacy NDC | 20230506_5e304da6-b541-4c10-b95a-27123c8508e7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0363-0705-78 | 00363070578 | 1 BOTTLE in 1 CARTON (0363-0705-78) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2021-10-31 | 0000-00-00 | No | No | Current |