Infants Ibuprofen
- Product NDC
- 71205-110
- 11-digit product format
- 712050110
- Labeler code
- 71205
- Product ID
- 71205-110_4f8063ab-d750-45b5-ae64-410900281562
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA079058
- Marketing category
- ANDA
- Marketing start
- 2010-05-11
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 50 mg/1.25mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 71205-110 | INFANTS IBUPROFEN (IBUPROFEN) SUSPENSION [PROFICIENT RX LP] | 2 | Legacy NDC | 20191122_d1fbc5ce-bd0e-4ac4-a77c-b159acfe7f4e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-110-15 | 71205011015 | 1 BOTTLE in 1 CARTON (71205-110-15) > 15 mL in 1 BOTTLE | 1 bottle | 2018-09-03 | 0000-00-00 | No | No | Current |
| 71205-110-30 | 71205011030 | 1 BOTTLE in 1 CARTON (71205-110-30) > 30 mL in 1 BOTTLE | 1 bottle | 2018-09-03 | 0000-00-00 | No | No | Current |