IBUPROFEN
- Product NDC
- 43063-936
- 11-digit product format
- 430630936
- Labeler code
- 43063
- Product ID
- 43063-936_e6daf710-dd5e-ef07-e053-2a95a90afb92
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- IBUPROFEN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA090796
- Marketing category
- ANDA
- Marketing start
- 2015-12-30
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 600 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43063-936 | IBUPROFEN TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.] | 13 | Legacy NDC | 20250105_e7d73293-bea0-4b07-a1b1-eaabb98c1b02.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-936-30 | 43063093630 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-936-30) | 2019-02-14 | 0000-00-00 | No | No | Current |