Ketorolac Tromethamine
- Product NDC
- 76045-209
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ketorolac Tromethamine
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Fresenius Kabi USA, LLC
- Application
- ANDA203242
- Marketing category
- ANDA
- Substance
- KETOROLAC TROMETHAMINE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 76045-209-10 | 24 BLISTER PACK in 1 CARTON (76045-209-10) / 1 SYRINGE, GLASS in 1 BLISTER PACK (76045-209-00) / 1 mL in 1 SYRINGE, GLASS | 2020-09-01 | | No | Historical |