Home
>
National Drug Code (NDC)
>
CROMOLYN SODIUM
CROMOLYN SODIUM - 42571-132-52 - (Cromolyn sodium)
Drug Information of CROMOLYN SODIUM
| Product NDC: | 42571-132 |
| Proprietary Name: | CROMOLYN SODIUM |
| Non Proprietary Name: | Cromolyn sodium |
| Active Ingredient(s): | 100 mg/5mL & nbsp; Cromolyn sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CROMOLYN SODIUM
| Product NDC: | 42571-132 |
| Labeler Name: | Micro Labs Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202745 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130504 |
Package Information of CROMOLYN SODIUM
| Package NDC: | 42571-132-52 |
| Package Description: | 96 CARTON in 1 CARTON (42571-132-52) > 1 TRAY in 1 CARTON (42571-132-51) > 8 AMPULE in 1 TRAY > 5 mL in 1 AMPULE (42571-132-21) |
NDC Information of CROMOLYN SODIUM
| NDC Code | 42571-132-52 |
| Proprietary Name | CROMOLYN SODIUM |
| Package Description | 96 CARTON in 1 CARTON (42571-132-52) > 1 TRAY in 1 CARTON (42571-132-51) > 8 AMPULE in 1 TRAY > 5 mL in 1 AMPULE (42571-132-21) |
| Product NDC | 42571-132 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cromolyn sodium |
| Dosage Form Name | SOLUTION, CONCENTRATE |
| Route Name | ORAL |
| Start Marketing Date | 20130504 |
| Marketing Category Name | ANDA |
| Labeler Name | Micro Labs Limited |
| Substance Name | CROMOLYN SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC] |
