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Chloroprocaine Hydrochloride
Chloroprocaine Hydrochloride - 55390-404-20 - (Chloroprocaine Hydrochloride)
Drug Information of Chloroprocaine Hydrochloride
| Product NDC: | 55390-404 |
| 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: | 55390-404 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040273 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19981101 |
Package Information of Chloroprocaine Hydrochloride
| Package NDC: | 55390-404-20 |
| Package Description: | 1 VIAL in 1 BOX (55390-404-20) > 20 mL in 1 VIAL |
NDC Information of Chloroprocaine Hydrochloride
| NDC Code | 55390-404-20 |
| Proprietary Name | Chloroprocaine Hydrochloride |
| Package Description | 1 VIAL in 1 BOX (55390-404-20) > 20 mL in 1 VIAL |
| Product NDC | 55390-404 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chloroprocaine Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | EPIDURAL; INFILTRATION |
| Start Marketing Date | 19981101 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | CHLOROPROCAINE HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Ester Local Anesthetic [EPC],Esters [Chemical/Ingredient],Local Anesthesia [PE] |
