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Chloroprocaine Hydrochloride
Chloroprocaine Hydrochloride - 0409-4170-01 - (CHLOROPROCAINE HYDROCHLORIDE)
Drug Information of Chloroprocaine Hydrochloride
| Product NDC: | 0409-4170 |
| Proprietary Name: | Chloroprocaine Hydrochloride |
| Non Proprietary Name: | CHLOROPROCAINE HYDROCHLORIDE |
| Active Ingredient(s): | 30 mg/mL & nbsp; CHLOROPROCAINE HYDROCHLORIDE |
| Administration Route(s): | EPIDURAL; INFILTRATION |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Chloroprocaine Hydrochloride
| Product NDC: | 0409-4170 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087446 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100324 |
Package Information of Chloroprocaine Hydrochloride
| Package NDC: | 0409-4170-01 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4170-01) > 30 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Chloroprocaine Hydrochloride
| NDC Code | 0409-4170-01 |
| Proprietary Name | Chloroprocaine Hydrochloride |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4170-01) > 30 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0409-4170 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CHLOROPROCAINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | EPIDURAL; INFILTRATION |
| Start Marketing Date | 20100324 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | CHLOROPROCAINE HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Ester Local Anesthetic [EPC],Esters [Chemical/Ingredient],Local Anesthesia [PE] |
