01 1ACETAMINOPHEN
02 7ACETAMINOPHEN; CODEINE PHOSPHATE
03 1ACETAMINOPHEN; HYDROCODONE BITARTRATE
04 1ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
05 1ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE; OXYCODONE TEREPHTHALATE
06 1ACETRIZOATE SODIUM
07 1ASPIRIN; METHOCARBAMOL
08 2CARBINOXAMINE MALEATE
09 1CHLORZOXAZONE
10 1DIENESTROL
11 6DIPHENHYDRAMINE HYDROCHLORIDE
12 3ESTRADIOL
13 8ETHINYL ESTRADIOL; NORETHINDRONE
14 2ETHINYL ESTRADIOL; NORGESTIMATE
15 1FLAVOXATE HYDROCHLORIDE
16 7HALOPERIDOL
17 1HALOPERIDOL LACTATE
18 13IBUPROFEN
19 1LEUPROLIDE ACETATE
20 6MESTRANOL; NORETHINDRONE
21 2METRONIDAZOLE
22 2MICONAZOLE NITRATE
23 1NICOTINE
24 1NONOXYNOL-9
25 5OFLOXACIN
26 1OXYBUTYNIN CHLORIDE
27 1PSEUDOEPHEDRINE HYDROCHLORIDE
28 5THEOPHYLLINE
29 3TOLMETIN SODIUM
30 2TRIPLE SULFA (SULFABENZAMIDE;SULFACETAMIDE;SULFATHIAZOLE)
01 1AEROSOL;VAGINAL
02 2CAPSULE, EXTENDED RELEASE;ORAL
03 7CAPSULE;ORAL
04 1CONCENTRATE;ORAL
05 1CREAM, SUPPOSITORY;TOPICAL, VAGINAL
06 2CREAM;VAGINAL
07 3ELIXIR;ORAL
08 1FILM, EXTENDED RELEASE;TRANSDERMAL
09 1IMPLANT;IMPLANTATION
10 9INJECTABLE;INJECTION
11 1SOLUTION;INTRAUTERINE
12 1SOLUTION;ORAL
13 1SUSPENSION/DROPS;ORAL
14 1SUSPENSION;ORAL
15 1SYRUP;ORAL
16 3SYSTEM;TRANSDERMAL
17 3TABLET, CHEWABLE;ORAL
18 1TABLET, EXTENDED RELEASE;ORAL
19 1TABLET; ORAL-21
20 1TABLET; ORAL-28
21 30TABLET;ORAL
22 9TABLET;ORAL-21
23 5TABLET;ORAL-28
24 1TABLET;VAGINAL
25 1TAMPON;VAGINAL
01 10.01%
02 20.035MG,0.035MG,0.035MG; 0.18MG,0.215MG,0.25MG
03 10.035MG,0.035MG;0.5MG,1MG
04 30.035MG,0.035MG;0.5MG,1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
05 10.035MG;0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
06 20.035MG;1MG
07 10.035MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 10.05MG/24HR
09 20.05MG;1MG
10 10.06MG;10MG
11 10.075MG/24HR
12 20.08MG;1MG
13 10.1MG/24HR
14 10.1MG;2MG
15 10.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
16 11.2GM;2%
17 5100MG
18 1100MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
19 1100MG/ML
20 110MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
21 110MG/ML
22 1112.5MG/15ML
23 112.5%
24 112.5MG/5ML
25 1120MG
26 1120MG/5ML;12MG/5ML
27 1125MG
28 115MG/16HR
29 1184MG;143.75MG;172.5MG
30 11MG
31 11MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
32 3200MG
33 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
34 120MG/ML
35 1225MG
36 2250MG
37 1250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
38 125MG
39 12MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
40 13.7%;2.86%;3.42%
41 1300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
42 1300MG;30MG
43 1300MG;60MG
44 1325MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
45 1325MG;30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
46 1325MG;400MG
47 1325MG;5MG
48 1325MG;60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
49 1325MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
50 1400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
51 2400MG/100ML
52 240MG/ML
53 14MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
54 14MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
55 14MG/ML
56 1500MG
57 1500MG;4.5MG;0.38MG
58 1500MG;5MG
59 250MG
60 250MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
61 153%
62 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
63 15MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
64 1600MG
65 1600MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
66 1800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
67 1EQ 200MG BASE
68 1EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
69 1EQ 400MG BASE
70 1EQ 600MG BASE
71 1EQ 65MG BASE
01 84DISCN
02 1OTC
03 3Blank
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : INJECTAPAP
Dosage Strength : 100MG/ML
Approval Date : 1986-03-07
Application Number : 17785
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET; ORAL
Proprietary Name : TYLENOL W/ CODEINE
Dosage Strength : 325MG;7.5MG **Federal Re...
Approval Date : 1982-01-01
Application Number : 85056
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET; ORAL
Proprietary Name : TYLENOL W/ CODEINE
Dosage Strength : 325MG;15MG **Federal Reg...
Approval Date : 1982-01-01
Application Number : 85056
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET; ORAL
Proprietary Name : TYLENOL W/ CODEINE
Dosage Strength : 325MG;30MG **Federal Reg...
Approval Date : 1982-01-01
Application Number : 85056
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET; ORAL
Proprietary Name : TYLENOL W/ CODEINE
Dosage Strength : 325MG;60MG **Federal Reg...
Approval Date : 1982-01-01
Application Number : 85056
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : SOLUTION; ORAL
Proprietary Name : TYLENOL W/ CODEINE
Dosage Strength : 120MG/5ML;12MG/5ML
Approval Date : 1982-01-01
Application Number : 85057
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : CAPSULE; ORAL
Proprietary Name : TYLENOL W/ CODEINE NO. 4
Dosage Strength : 300MG;60MG
Approval Date : 1982-01-01
Application Number : 87421
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : CAPSULE; ORAL
Proprietary Name : TYLENOL W/ CODEINE NO. 3
Dosage Strength : 300MG;30MG
Approval Date : 1982-01-01
Application Number : 87422
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Dosage Form : TABLET; ORAL
Proprietary Name : TYCOLET
Dosage Strength : 500MG;5MG
Approval Date : 1986-08-27
Application Number : 89385
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Dosage Form : CAPSULE; ORAL
Proprietary Name : TYLOX-325
Dosage Strength : 325MG;5MG
Approval Date : 1984-11-08
Application Number : 88246
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Mcneil Consumer Health is a supplier offers 3 products (APIs, Excipients or Intermediates).
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