Ibuprofen
- Product NDC
- 50090-5432
- 11-digit product format
- 500905432
- Labeler code
- 50090
- Product ID
- 50090-5432_fa9d253f-3565-47ac-8457-8e8d276d6416
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA213794
- Marketing category
- ANDA
- Marketing start
- 2020-05-08
- 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5432 | IBUPROFEN TABLET [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC | 20210417_a0b1a685-9334-4eab-8cc0-a3d4bd60e149.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5432-0 | 50090543200 | 30 TABLET in 1 BOTTLE (50090-5432-0) | 30 tablet | 2021-01-18 | 0000-00-00 | No | No | Current |