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NDC | HCPCS | HCPCS Description | NDC Label | Route of Administration |
|---|---|---|---|---|
50268-0761-12 | None | TEMOZOLOMIDE, 20 MG, ORAL | TEMOZOLOMIDE (4 X 5) 20 MG | PO |
50268-0762-11 | None | TEMOZOLOMIDE, 100 MG, ORAL | TEMOZOLOMIDE (INNERPACK) 100 MG | PO |
50268-0762-12 | None | TEMOZOLOMIDE, 100 MG, ORAL | TEMOZOLOMIDE 100 MG | PO |
50268-0763-11 | None | TEMOZOLOMIDE, 20 MG, ORAL | TEMOZOLOMIDE (INNERPACK) 140 MG | PO |
50268-0763-12 | None | TEMOZOLOMIDE, 20 MG, ORAL | TEMOZOLOMIDE 140 MG | PO |
50383-0040-04 | J7510 | PREDNISOLONE ORAL, PER 5 MG | PREDNISOLONE SODIUM PHOSPHATE (AF,SF,DYE-FREE) 5 MG/5 ML | PO |
50383-0042-24 | J7510 | PREDNISOLONE ORAL, PER 5 MG | PREDNISOLONE 15 MG/5 ML | PO |
50383-0042-48 | J7510 | PREDNISOLONE ORAL, PER 5 MG | PREDNISOLONE 15 MG/5 ML | PO |
50383-0741-20 | J7611 | ALBUTEROL, INHALATION SOLUTION, FDA-APPROVED FINAL PRODUCT, NON-COMPOUNDED, ADMINISTERED THROUGH DME, CONCENTRATED FORM, 1 MG | ALBUTEROL SULFATE 0.5% | IH |
50383-0801-16 | Q0169 | PROMETHAZINE HYDROCHLORIDE, 12.5 MG, ORAL, FDA APPROVED PRESCRIPTION ANTI-EMETIC, FOR USE AS A COMPLETE THERAPEUTIC SUBSTITUTE FOR AN IV ANTI-EMETIC AT THE TIME OF CHEMOTHERAPY TREATMENT, NOT TO EXCEED A 48 HOUR DOSAGE REGIMEN | PROMETHAZINE HCL (CHERRY) 6.25 MG/5 ML | PO |
50383-0810-16 | J8499 | PRESCRIPTION DRUG, ORAL, NON CHEMOTHERAPEUTIC, NOS | ACYCLOVIR (BANANA) 200 MG/5 ML | PO |
50419-0385-01 | J3490 | UNCLASSIFIED DRUGS | ALIQOPA (LYOPHILIZED) 60 MG | IV |
HCPCS Code | Description | Billing Unit | SA Type |
|---|---|---|---|
A7005 | Administration set, with small volume nonfiltered pneumatic nebulizer, non-disposable | Each | N |
A7006 | Administration set, with small volume filter pneumatic nebulizer | Each | N |
A7007 | Large voume nebulizer, disposable, unfilled, used with aerosol compressor | Each | N |
A7008 | Large volume nebulizer, disposable, Prefilled, used with aerosol compressor | Each | N |
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