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Diclofenac Sodium
Diclofenac Sodium - 21695-710-25 - (Diclofenac Sodium)
Drug Information of Diclofenac Sodium
| Product NDC: | 21695-710 |
| Proprietary Name: | Diclofenac Sodium |
| Non Proprietary Name: | Diclofenac Sodium |
| Active Ingredient(s): | 1 mg/mL & nbsp; Diclofenac Sodium |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diclofenac Sodium
| Product NDC: | 21695-710 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078792 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20071228 |
Package Information of Diclofenac Sodium
| Package NDC: | 21695-710-25 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (21695-710-25) > 2.5 mL in 1 BOTTLE, DROPPER |
NDC Information of Diclofenac Sodium
| NDC Code | 21695-710-25 |
| Proprietary Name | Diclofenac Sodium |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (21695-710-25) > 2.5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 21695-710 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diclofenac Sodium |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20071228 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | DICLOFENAC SODIUM |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
