Ibuprofen
- Product NDC
- 50804-217
- 11-digit product format
- 508040217
- Labeler code
- 50804
- Product ID
- 50804-217_ccc52d86-bc67-4730-bb5e-55197d4569f5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Good Sense (Geiss, Destin & Dunn, Inc.)
- Application
- ANDA079174
- Marketing category
- ANDA
- Marketing start
- 2013-04-13
- Marketing end
- 2021-12-30
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50804-217-50 | 50804021750 | 1 BOTTLE, PLASTIC in 1 BOX (50804-217-50) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC | 2013-04-13 | 2021-12-30 | No | No | Current |