Diclofenac Sodium D/R is a Oral Tablet, Delayed Release in the Human Prescription Drug category. It is labeled and distributed by Direct Rx. The primary component is Diclofenac Sodium.
Product ID | 61919-075_3fdaa3f6-dd9d-6a74-e054-00144ff88e88 |
NDC | 61919-075 |
Product Type | Human Prescription Drug |
Proprietary Name | Diclofenac Sodium D/R |
Generic Name | Diclofenac Sodium D/r |
Dosage Form | Tablet, Delayed Release |
Route of Administration | ORAL |
Marketing Start Date | 2014-01-01 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA075185 |
Labeler Name | Direct RX |
Substance Name | DICLOFENAC SODIUM |
Active Ingredient Strength | 75 mg/1 |
Pharm Classes | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC] |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 2014-01-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA075185 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-01-01 |
Marketing Category | ANDA |
Application Number | ANDA075185 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2019-08-16 |
Marketing Category | ANDA |
Application Number | ANDA075185 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-08-16 |
Marketing Category | ANDA |
Application Number | ANDA075185 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-01-01 |
Ingredient | Strength |
---|---|
DICLOFENAC SODIUM | 75 mg/1 |
SPL SET ID: | 2ae3c1e2-f053-4efb-9597-eeac4998d23f |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
61919-074 | Diclofenac Sodium D/R | Diclofenac Sodium D/R |
61919-075 | Diclofenac Sodium D/R | Diclofenac Sodium D/R |
61919-060 | VOLTAREN | DICLOFENAC SODIUM D/R |