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"68001-201-08" National Drug Code (NDC)
Diclofenac Sodium 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-201-08)
(BluePoint Laboratories)
NDC Code
68001-201-08
Package Description
1000 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-201-08)
Product NDC
68001-201
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Diclofenac Sodium
Non-Proprietary Name
Diclofenac Sodium
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20140224
Marketing Category Name
ANDA
Application Number
ANDA074376
Manufacturer
BluePoint Laboratories
Substance Name
DICLOFENAC SODIUM
Strength
50
Strength Unit
mg/1
Pharmacy Classes
Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68001-201-08