• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

FDA Application

  • Print
  • Share
  • E-mail
-

NDC Search Results on Active Ingredient: aspirin

Click on Active Ingredient to view the label.

Ingredient Name NDC Company Name Application Number or Regulatory Citation Product Type Marketing Category
ASPIRIN 64092-150-36  GREAT LAKES WHOLESALE, MARKETING, & SALES, INC.  part343  HUMAN OTC DRUG  OTC monograph not final 
ASPIRIN 37808-157-14  H E B  M013  HUMAN OTC DRUG  OTC Monograph Drug 
ASPIRIN 37808-630-30  H E B  M013  HUMAN OTC DRUG  OTC Monograph Drug 
ASPIRIN 37808-157-12  H E B  M013  HUMAN OTC DRUG  OTC Monograph Drug 
ASPIRIN; ACETAMINOPHEN; CAFFEINE 37808-586-80  H E B  M013  HUMAN OTC DRUG  OTC Monograph Drug 
ASPIRIN 37808-031-87  H E B  part343  HUMAN OTC DRUG  OTC monograph not final 
ASPIRIN 37808-157-17  H E B  M013  HUMAN OTC DRUG  OTC Monograph Drug 
ACETAMINOPHEN; CAFFEINE; ASPIRIN 37808-374-78  H E B  ANDA075794  HUMAN OTC DRUG  ANDA 
ASPIRIN 37808-031-78  H E B  part343  HUMAN OTC DRUG  OTC monograph not final 
ASPIRIN 37808-600-32  H E B  M013  HUMAN OTC DRUG  OTC Monograph Drug 
ASPIRIN 37808-031-90  H E B  part343  HUMAN OTC DRUG  OTC monograph not final 
ASPIRIN 37808-867-30  H E B  M013  HUMAN OTC DRUG  OTC Monograph Drug 
ASPIRIN; ACETAMINOPHEN; CAFFEINE 37808-586-20  H E B  M013  HUMAN OTC DRUG  OTC Monograph Drug 
PHENYLEPHRINE BITARTRATE; CHLORPHENIRAMINE MALEATE; ASPIRIN 37808-768-20  H. E. Butt Grocery Company  part341  HUMAN OTC DRUG  OTC monograph final 
ASPIRIN; ANHYDROUS CITRIC ACID; SODIUM BICARBONATE 37808-421-68  H. E. Butt Grocery Company  part343  HUMAN OTC DRUG  OTC monograph final 
ANHYDROUS CITRIC ACID; SODIUM BICARBONATE; ASPIRIN 37808-540-24  H. E. Butt Grocery Company  505G(a)(3)  HUMAN OTC DRUG  OTC Monograph Drug 
ASPIRIN 52959-018-40  H.J. Harkins Company Inc. dba Pharma Pac  part343  HUMAN OTC DRUG  OTC monograph final 
ASPIRIN 52959-018-80  H.J. Harkins Company Inc. dba Pharma Pac  part343  HUMAN OTC DRUG  OTC monograph final 
CAFFEINE; ASPIRIN; BUTALBITAL 52959-370-00  H.J. Harkins Company Inc. dba Pharma Pac  ANDA086162  HUMAN PRESCRIPTION DRUG  ANDA 
CAFFEINE; ASPIRIN; BUTALBITAL 52959-370-25  H.J. Harkins Company Inc. dba Pharma Pac  ANDA086162  HUMAN PRESCRIPTION DRUG  ANDA 
ASPIRIN 52959-018-00  H.J. Harkins Company Inc. dba Pharma Pac  part343  HUMAN OTC DRUG  OTC monograph final 
CAFFEINE; ASPIRIN; BUTALBITAL 52959-370-12  H.J. Harkins Company Inc. dba Pharma Pac  ANDA086162  HUMAN PRESCRIPTION DRUG  ANDA 
CAFFEINE; ASPIRIN; BUTALBITAL 52959-370-30  H.J. Harkins Company Inc. dba Pharma Pac  ANDA086162  HUMAN PRESCRIPTION DRUG  ANDA 
CAFFEINE; ASPIRIN; BUTALBITAL 52959-370-50  H.J. Harkins Company Inc. dba Pharma Pac  ANDA086162  HUMAN PRESCRIPTION DRUG  ANDA 
CAFFEINE; ASPIRIN; BUTALBITAL 52959-370-20  H.J. Harkins Company Inc. dba Pharma Pac  ANDA086162  HUMAN PRESCRIPTION DRUG  ANDA 
ASPIRIN 52959-018-20  H.J. Harkins Company Inc. dba Pharma Pac  part343  HUMAN OTC DRUG  OTC monograph final 
CAFFEINE; ASPIRIN; BUTALBITAL 52959-370-90  H.J. Harkins Company Inc. dba Pharma Pac  ANDA086162  HUMAN PRESCRIPTION DRUG  ANDA 
ASPIRIN 52959-018-30  H.J. Harkins Company Inc. dba Pharma Pac  part343  HUMAN OTC DRUG  OTC monograph final 
ASPIRIN 52959-018-60  H.J. Harkins Company Inc. dba Pharma Pac  part343  HUMAN OTC DRUG  OTC monograph final 
CAFFEINE; ASPIRIN; BUTALBITAL 52959-370-60  H.J. Harkins Company Inc. dba Pharma Pac  ANDA086162  HUMAN PRESCRIPTION DRUG  ANDA 
1-30 31-60 61-90 91-120 121-150 151-180 181-210 211-240 241-270 271-300
301-330 331-360 361-390 391-420 421-450 451-480 481-510 511-540 541-570 571-600
601-630 631-660 661-690 691-720 721-750 751-780 781-810 811-840 841-870 871-900
901-930 931-960 961-990 991-1020 1021-1050 1051-1080 1081-1110 1111-1140 1141-1170 1171-1200
1201-1230 1231-1260 1261-1290 1291-1320 1321-1350 1351-1380 1381-1410 1411-1440 1441-1470 1471-1500
1501-1530 1531-1560 1561-1590 1591-1620 1621-1650 1651-1680 1681-1710 1711-1740 1741-1770 1771-1800
1801-1830 1831-1860 1861-1890 1891-1920 1921-1950 1951-1980 1981-2010 2011-2034

Return to the FDA Label Search Page

-
-