IBU
- Product NDC
- 60760-135
- 11-digit product format
- 607600135
- Labeler code
- 60760
- Product ID
- 60760-135_7ad086e3-91fd-fcb7-e053-2a91aa0acdfe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary
- Application
- ANDA075682
- Marketing category
- ANDA
- Marketing start
- 2016-01-08
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 800 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-135-00 | 60760013500 | 100 TABLET in 1 BOTTLE, PLASTIC (60760-135-00) | 100 tablet | 2016-01-08 | 0000-00-00 | No | No | Current |
| 60760-135-09 | 60760013509 | 9 TABLET in 1 BOTTLE, PLASTIC (60760-135-09) | 9 tablet | 2016-10-14 | 0000-00-00 | No | No | Current |
| 60760-135-20 | 60760013520 | 20 TABLET in 1 BOTTLE, PLASTIC (60760-135-20) | 20 tablet | 2016-01-11 | 0000-00-00 | No | No | Current |
| 60760-135-30 | 60760013530 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-135-30) | 30 tablet | 2016-01-11 | 0000-00-00 | No | No | Current |
| 60760-135-60 | 60760013560 | 60 TABLET in 1 BOTTLE, PLASTIC (60760-135-60) | 60 tablet | 2016-02-29 | 0000-00-00 | No | No | Current |
| 60760-135-90 | 60760013590 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-135-90) | 90 tablet | 2016-09-06 | 0000-00-00 | No | No | Current |