Ibuprofen
- Product NDC
- 50090-2670
- 11-digit product format
- 500902670
- Labeler code
- 50090
- Product ID
- 50090-2670_07c0b932-565b-4c9d-af48-d084add80088
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091625
- Marketing category
- ANDA
- Marketing start
- 2015-12-21
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 600 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2670-0 | 50090267000 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-2670-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 30 blister pack | 2016-12-02 | 0000-00-00 | No | No | Current |