Ibuprofen
- Product NDC
- 55700-694
- 11-digit product format
- 557000694
- Labeler code
- 55700
- Product ID
- 55700-694_aa3b6559-8545-4d95-87b3-69847acbbf41
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA091625
- Marketing category
- ANDA
- Marketing start
- 2018-10-26
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 400 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-694-30 | 55700069430 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-694-30) | 2018-10-26 | 0000-00-00 | No | No | Current |
| 55700-694-60 | 55700069460 | 60 TABLET, FILM COATED in 1 BOTTLE (55700-694-60) | 2020-12-10 | 0000-00-00 | No | No | Current |
| 55700-694-90 | 55700069490 | 90 TABLET, FILM COATED in 1 BOTTLE (55700-694-90) | 2020-12-10 | 0000-00-00 | No | No | Current |