ibuprofen
- Product NDC
- 30142-495
- 11-digit product format
- 301420495
- Labeler code
- 30142
- Product ID
- 30142-495_be5bc6fe-e14d-438f-bab4-0e0a8d1728cd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- ANDA072096
- Marketing category
- ANDA
- Marketing start
- 2015-08-28
- Marketing end
- 2023-03-31
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- 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 |
|---|
| 30142-495-78 | 30142049578 | 100 TABLET, FILM COATED in 1 BOTTLE (30142-495-78) | 2015-08-28 | 0000-00-00 | No | No | Current |
| 30142-495-82 | 30142049582 | 200 TABLET, FILM COATED in 1 BOTTLE (30142-495-82) | 2019-11-14 | 0000-00-00 | No | No | Current |