Product NDC: | 55390-403 |
Proprietary Name: | Chloroprocaine Hydrochloride |
Non Proprietary Name: | Chloroprocaine Hydrochloride |
Active Ingredient(s): | 20 mg/mL & nbsp; Chloroprocaine Hydrochloride |
Administration Route(s): | EPIDURAL; INFILTRATION |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55390-403 |
Labeler Name: | Bedford Laboratories |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040273 |
Marketing Category: | ANDA |
Start Marketing Date: | 19981101 |
Package NDC: | 55390-403-20 |
Package Description: | 1 VIAL in 1 BOX (55390-403-20) > 20 mL in 1 VIAL |
NDC Code | 55390-403-20 |
Proprietary Name | Chloroprocaine Hydrochloride |
Package Description | 1 VIAL in 1 BOX (55390-403-20) > 20 mL in 1 VIAL |
Product NDC | 55390-403 |
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 | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Ester Local Anesthetic [EPC],Esters [Chemical/Ingredient],Local Anesthesia [PE] |