Sunmark ibuprofen ib
- Product NDC
- 49348-927
- 11-digit product format
- 493480927
- Labeler code
- 49348
- Product ID
- 49348-927_ef713d42-5595-487a-869f-c704f0ba0a7f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA077349
- Marketing category
- ANDA
- Marketing start
- 2006-03-20
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49348-927-09 | 49348092709 | 1 BOTTLE in 1 CARTON (49348-927-09) > 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2006-03-27 | 0000-00-00 | No | No | Current |
| 49348-927-10 | 49348092710 | 1 BOTTLE in 1 CARTON (49348-927-10) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2006-03-20 | 0000-00-00 | No | No | Current |