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ACULAR LS
ACULAR LS - 0023-9277-05 - (ketorolac tromethamine)
Drug Information of ACULAR LS
| Product NDC: | 0023-9277 |
| Proprietary Name: | ACULAR LS |
| Non Proprietary Name: | ketorolac tromethamine |
| Active Ingredient(s): | 4 mg/mL & nbsp; ketorolac tromethamine |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ACULAR LS
| Product NDC: | 0023-9277 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021528 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030819 |
Package Information of ACULAR LS
| Package NDC: | 0023-9277-05 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (0023-9277-05) > 5 mL in 1 BOTTLE, DROPPER |
NDC Information of ACULAR LS
| NDC Code | 0023-9277-05 |
| Proprietary Name | ACULAR LS |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (0023-9277-05) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 0023-9277 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ketorolac tromethamine |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20030819 |
| Marketing Category Name | NDA |
| Labeler Name | Allergan, Inc. |
| Substance Name | KETOROLAC TROMETHAMINE |
| Strength Number | 4 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
