CHILDRENS IBUPROFEN
- Product NDC
- 58602-212
- 11-digit product format
- 586020212
- Labeler code
- 58602
- Product ID
- 58602-212_57bcf51e-e754-41c3-ac21-aa3bb0a05045
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Aurohealth LLC
- Application
- ANDA209179
- Marketing category
- ANDA
- Marketing start
- 2018-04-17
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 100 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 58602-212-20 | 58602021220 | 1 BOTTLE in 1 CARTON (58602-212-20) > 240 mL in 1 BOTTLE | 1 bottle | 2018-04-17 | 0000-00-00 | No | No | Current |
| 58602-212-24 | 58602021224 | 1 BOTTLE in 1 CARTON (58602-212-24) > 120 mL in 1 BOTTLE | 1 bottle | 2018-04-17 | 0000-00-00 | No | No | Current |