Ibuprofen
- Product NDC
- 48792-7812
- 11-digit product format
- 487927812
- Labeler code
- 48792
- Product ID
- 48792-7812_84f5a057-bb87-2c2b-e053-2991aa0ad665
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sunshine Lake Pharma Co., Ltd.
- Application
- ANDA204062
- Marketing category
- ANDA
- Marketing start
- 2018-09-24
- 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
- 2020-12-31
- 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 |
|---|
| 48792-7812 | IBUPROFEN TABLET, FILM COATED [SUNSHINE LAKE PHARMA CO., LTD.] | 6 | Legacy NDC | 20241210_76ad62e9-4784-fe61-e053-2a91aa0aee8b.zip |