FDA Application
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NDC Search Results on Active Ingredient: codeine
Click on Active Ingredient to view the label.
Ingredient Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
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CODEINE PHOSPHATE; ACETAMINOPHEN | 33261-002-50 | Aidarex Pharmaceuticals LLC | ANDA089828 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 33261-002-02 | Aidarex Pharmaceuticals LLC | ANDA089828 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 33261-001-28 | Aidarex Pharmaceuticals LLC | ANDA089805 | HUMAN PRESCRIPTION DRUG | ANDA |
PROMETHAZINE HYDROCHLORIDE; CODEINE PHOSPHATE; PHENYLEPHRINE HYDROCHLORIDE | 50383-805-16 | Akorn | ANDA040674 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 50383-337-06 | Akorn | ANDA040119 | HUMAN PRESCRIPTION DRUG | ANDA |
PROMETHAZINE HYDROCHLORIDE; CODEINE PHOSPHATE; PHENYLEPHRINE HYDROCHLORIDE | 50383-805-04 | Akorn | ANDA040674 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 50383-338-10 | Akorn | ANDA040119 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 50383-340-15 | Akorn | ANDA040119 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 50383-339-12 | Akorn | ANDA040119 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 50383-079-16 | Akorn | ANDA040119 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 50383-340-17 | Akorn | ANDA040119 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; PROMETHAZINE HYDROCHLORIDE | 50383-804-16 | Akorn | ANDA040151 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; PROMETHAZINE HYDROCHLORIDE | 50383-804-04 | Akorn | ANDA040151 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 50383-338-11 | Akorn | ANDA040119 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 50383-339-13 | Akorn | ANDA040119 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 50383-337-05 | Akorn | ANDA040119 | HUMAN PRESCRIPTION DRUG | ANDA |
GUAIFENESIN; CODEINE PHOSPHATE | 50383-087-07 | Akorn Operating Company LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
GUAIFENESIN; CODEINE PHOSPHATE | 50383-087-04 | Akorn Operating Company LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
GUAIFENESIN; CODEINE PHOSPHATE | 50383-087-10 | Akorn Operating Company LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
GUAIFENESIN; CODEINE PHOSPHATE | 50383-087-05 | Akorn Operating Company LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
GUAIFENESIN; CODEINE PHOSPHATE | 50383-087-16 | Akorn Operating Company LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
GUAIFENESIN; CODEINE PHOSPHATE | 50383-087-12 | Akorn Operating Company LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
CODEINE PHOSPHATE; ACETAMINOPHEN | 60687-615-01 | American Health Packaging | ANDA202800 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 60687-615-11 | American Health Packaging | ANDA202800 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 60687-604-11 | American Health Packaging | ANDA202800 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 60687-604-01 | American Health Packaging | ANDA202800 | HUMAN PRESCRIPTION DRUG | ANDA |
PROMETHAZINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE; CODEINE PHOSPHATE | 65162-694-86 | Amneal Pharmaceuticals LLC | ANDA200963 | HUMAN PRESCRIPTION DRUG | ANDA |
PROMETHAZINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE; CODEINE PHOSPHATE | 65162-694-90 | Amneal Pharmaceuticals LLC | ANDA200963 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 65162-033-10 | Amneal Pharmaceuticals LLC | ANDA040779 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 65162-033-11 | Amneal Pharmaceuticals LLC | ANDA040779 | HUMAN PRESCRIPTION DRUG | ANDA |
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301-330 | 331-360 | 361-390 | 391-420 | 421-450 | 451-480 | 481-510 | 511-540 | 541-570 | 571-600 |
601-630 | 631-660 | 661-690 | 691-720 | 721-750 | 751-764 |
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