IBUPROFEN
- Product NDC
- 29485-7625
- 11-digit product format
- 294857625
- Labeler code
- 29485
- Product ID
- 29485-7625_b45032ce-c235-6104-e053-2a95a90a9f22
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IBUPROFEN 200MG
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mechanical Servants LLC
- Application
- ANDA079174
- Marketing category
- ANDA
- Marketing start
- 2019-03-13
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 29485-7625-6 | 29485762506 | 3 POUCH in 1 PACKAGE (29485-7625-6) > 2 TABLET, FILM COATED in 1 POUCH | 3 pouch | 2019-03-13 | 0000-00-00 | No | No | Current |