Ibuprofen
- Product NDC
- 21130-921
- 11-digit product format
- 211300921
- Labeler code
- 21130
- Product ID
- 21130-921_18fad17b-c344-453c-a5e9-ef5fbe0db931
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Better Living Brands, LLC
- Application
- ANDA075010
- Marketing category
- ANDA
- Marketing start
- 1988-05-24
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 21130-921-03 | 21130092103 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (21130-921-03) | 1988-05-24 | 0000-00-00 | No | No | Current |
| 21130-921-15 | 21130092115 | 1 BOTTLE, PLASTIC in 1 CARTON (21130-921-15) > 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 1988-05-24 | 0000-00-00 | No | No | Current |