Ketorolac Tromethamine
- Product NDC
- 68071-2569
- 11-digit product format
- 680712569
- Labeler code
- 68071
- Product ID
- 68071-2569_d2814bd0-6a16-29c7-e053-2995a90af671
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ketorolac Tromethamine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA210616
- Marketing category
- ANDA
- Marketing start
- 2018-10-11
- Marketing end
- 0000-00-00
- Substance
- KETOROLAC TROMETHAMINE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC],Cyclooxygenase Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2569-8 | 68071256908 | 8 TABLET, FILM COATED in 1 BOTTLE (68071-2569-8) | 2021-12-06 | 0000-00-00 | No | No | Current |