Ibuprofen
- Product NDC
- 33992-0393
- 11-digit product format
- 339920393
- Labeler code
- 33992
- Product ID
- 33992-0393_9eeb559b-72f1-48a6-bac9-a79a56c71f9c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- GREENBRIER INTERNATIONAL, INC.
- Application
- ANDA075139
- Marketing category
- ANDA
- Marketing start
- 1999-03-01
- 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 |
|---|
| 33992-0393-1 | 33992039301 | 1 BOTTLE in 1 CARTON (33992-0393-1) > 40 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 1999-03-01 | 0000-00-00 | No | No | Current |
| 33992-0393-2 | 33992039302 | 1 BOTTLE in 1 CARTON (33992-0393-2) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 1999-03-01 | 2022-02-06 | No | No | Current |