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Diclofenac Sodium
Diclofenac Sodium - 51079-224-20 - (diclofenac sodium)
Drug Information of Diclofenac Sodium
| Product NDC: | 51079-224 |
| Proprietary Name: | Diclofenac Sodium |
| Non Proprietary Name: | diclofenac sodium |
| Active Ingredient(s): | 75 mg/1 & nbsp; diclofenac sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diclofenac Sodium
| Product NDC: | 51079-224 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075281 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100604 |
Package Information of Diclofenac Sodium
| Package NDC: | 51079-224-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-224-20) > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (51079-224-01) |
NDC Information of Diclofenac Sodium
| NDC Code | 51079-224-20 |
| Proprietary Name | Diclofenac Sodium |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-224-20) > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (51079-224-01) |
| Product NDC | 51079-224 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | diclofenac sodium |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100604 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | DICLOFENAC SODIUM |
| Strength Number | 75 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
