FDA Label Search
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NDC Search Results on Proprietary Name: tylenol
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Proprietary Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
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Motrin Dual Action With Tylenol | 50580-208-16 | Johnson & Johnson Consumer Inc. | ANDA214836 | HUMAN OTC DRUG | ANDA |
TYLENOL 8 HR ARTHRITIS PAIN | 50580-575-01 | Johnson & Johnson Consumer Inc. | ANDA211544 | HUMAN OTC DRUG | ANDA |
TYLENOL with Codeine | 50090-0006-2 | A-S Medication Solutions | ANDA085055 | HUMAN PRESCRIPTION DRUG | ANDA |
Motrin Dual Action With Tylenol | 50580-208-12 | Johnson & Johnson Consumer Inc. | ANDA214836 | HUMAN OTC DRUG | ANDA |
TYLENOL 8 HR ARTHRITIS PAIN | 50580-575-02 | Johnson & Johnson Consumer Inc. | ANDA211544 | HUMAN OTC DRUG | ANDA |
TYLENOL 8 HR MUSCLE ACHES AND PAIN | 50580-576-02 | Johnson & Johnson Consumer Inc. | ANDA211544 | HUMAN OTC DRUG | ANDA |
TYLENOL 8 HR ARTHRITIS PAIN | 50580-575-03 | Johnson & Johnson Consumer Inc. | ANDA211544 | HUMAN OTC DRUG | ANDA |
TYLENOL 8 HR ARTHRITIS PAIN | 50580-575-06 | Johnson & Johnson Consumer Inc. | ANDA211544 | HUMAN OTC DRUG | ANDA |
Motrin Dual Action With Tylenol | 50580-208-02 | Johnson & Johnson Consumer Inc. | ANDA214836 | HUMAN OTC DRUG | ANDA |
TYLENOL 8 HR MUSCLE ACHES AND PAIN | 50580-576-01 | Johnson & Johnson Consumer Inc. | ANDA211544 | HUMAN OTC DRUG | ANDA |
Motrin Dual Action With Tylenol | 50580-208-08 | Johnson & Johnson Consumer Inc. | ANDA214836 | HUMAN OTC DRUG | ANDA |
Tylenol 8 HR Arthritis Pain | 50580-783-32 | Johnson & Johnson Consumer Inc. | NDA019872 | HUMAN OTC DRUG | NDA |
Tylenol 8 HR Arthritis Pain | 50580-783-30 | Johnson & Johnson Consumer Inc. | NDA019872 | HUMAN OTC DRUG | NDA |
Tylenol 8 HR Arthritis Pain | 50580-783-29 | Johnson & Johnson Consumer Inc. | NDA019872 | HUMAN OTC DRUG | NDA |
Tylenol 8 HR Arthritis Pain | 50580-783-31 | Johnson & Johnson Consumer Inc. | NDA019872 | HUMAN OTC DRUG | NDA |
Tylenol 8 HR Arthritis Pain | 50580-783-25 | Johnson & Johnson Consumer Inc. | NDA019872 | HUMAN OTC DRUG | NDA |
Tylenol 8HR | 50580-309-02 | Johnson & Johnson Consumer Inc. | NDA019872 | HUMAN OTC DRUG | NDA |
Tylenol 8 HR Arthritis Pain | 50580-783-10 | Johnson & Johnson Consumer Inc. | NDA019872 | HUMAN OTC DRUG | NDA |
Tylenol 8 HR Arthritis Pain | 50580-783-24 | Johnson & Johnson Consumer Inc. | NDA019872 | HUMAN OTC DRUG | NDA |
Tylenol 8HR | 50580-309-01 | Johnson & Johnson Consumer Inc. | NDA019872 | HUMAN OTC DRUG | NDA |
TYLENOL EXTRA STRENGTH | 70264-027-01 | R J General Corporation | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
Tylenol Extra Strength | 50269-449-25 | JC World Bell Wholesale Co., Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
Childrens TYLENOL | 50580-555-05 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
Tylenol Extra Strength | 50580-472-01 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
TYLENOL Cold Plus Flu Severe | 50580-402-02 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
Tylenol Extra Strength | 50580-937-06 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
Tylenol Sinus Severe | 50580-507-04 | Johnson & Johnson Consumer Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
Tylenol Sinus Severe, TRAVEL BASIX | 66715-7857-2 | Lil Drug Store Products, Inc | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
TYLENOL Extra Strength | 50580-590-02 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
Tylenol PM Extra Strength | 50580-608-02 | Johnson & Johnson Consumer Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
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