01 1ACETAMINOPHEN; CODEINE PHOSPHATE
02 1AMANTADINE HYDROCHLORIDE
03 2BENZTHIAZIDE
04 4BUTABARBITAL SODIUM
05 4DEXAMETHASONE
06 1DIENESTROL
07 2DYDROGESTERONE
08 1ERYTHROMYCIN
09 4ESTROGENS, ESTERIFIED
10 4FLUVOXAMINE MALEATE
11 3HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
12 4HYDRALAZINE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE; RESERPINE
13 2HYDROCHLOROTHIAZIDE
14 3HYDROCORTISONE
15 3LACTULOSE
16 1LEVONORDEFRIN; MEPIVACAINE HYDROCHLORIDE
17 2LITHIUM CARBONATE
18 1LITHIUM CITRATE
19 1MEDROXYPROGESTERONE ACETATE
20 1MEPIVACAINE HYDROCHLORIDE
21 3MEPROBAMATE
22 2METHOCARBAMOL
23 2PHENDIMETRAZINE TARTRATE
24 1PHENTERMINE HYDROCHLORIDE
25 1PIPERAZINE CITRATE
26 5PREDNISONE
27 1PYRIDOSTIGMINE BROMIDE
28 5QUINIDINE SULFATE
29 2RAUWOLFIA SERPENTINA ROOT
30 1RESERPINE
31 1SULFASALAZINE
32 1SULFISOXAZOLE
33 2TETRACYCLINE HYDROCHLORIDE
34 1TRIAMCINOLONE ACETONIDE
01 11CAPSULE;ORAL
02 1CREAM;TOPICAL
03 1CREAM;VAGINAL
04 2INJECTABLE;INJECTION
05 3LOTION;TOPICAL
06 1SOLUTION;ORAL
07 2SOLUTION;ORAL, RECTAL
08 2SYRUP;ORAL
09 1TABLET, DELAYED RELEASE;ORAL
10 49TABLET;ORAL
01 10.01%
02 10.05MG/ML;2%
03 10.1%
04 10.25MG
05 10.3MG
06 10.5%
07 10.5MG
08 10.625MG
09 10.75MG
10 21%
11 11.25MG
12 11.5MG
13 3100MG
14 1100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
15 1100MG;50MG
16 310GM/15ML
17 210MG
18 110MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
19 1150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 116.2MG
21 11MG
22 12.5MG
23 3200MG
24 120MG
25 2250MG
26 225MG
27 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
28 425MG;15MG;0.1MG
29 125MG;25MG
30 13%
31 4300MG
32 130MG
33 132.4MG
34 1325MG;30MG
35 235MG
36 2400MG
37 148.6MG
38 14MG
39 4500MG
40 450MG
41 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
42 150MG;50MG
43 15MG
44 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
45 1750MG
46 18MG
47 197.2MG
48 1EQ 300MG CARBONATE/5ML
49 1EQ 500MG BASE/5ML
01 73DISCN
RLD : No
TE Code :
ACETAMINOPHEN; CODEINE PHOSPHATE
Solvay Chemicals International S.A
Dosage Form : CAPSULE; ORAL
Proprietary Name : PROVAL #3
Dosage Strength : 325MG;30MG
Approval Date : 1982-01-01
Application Number : 85685
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Solvay Chemicals International S.A
Dosage Form : CAPSULE; ORAL
Proprietary Name : SYMADINE
Dosage Strength : 100MG
Approval Date : 1986-09-04
Application Number : 71000
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Solvay Chemicals International S.A
Dosage Form : TABLET; ORAL
Proprietary Name : AQUATAG
Dosage Strength : 25MG
Approval Date : 1982-01-01
Application Number : 16001
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Solvay Chemicals International S.A
Dosage Form : TABLET; ORAL
Proprietary Name : AQUATAG
Dosage Strength : 50MG
Approval Date : 1982-01-01
Application Number : 16001
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Solvay Chemicals International S.A
Dosage Form : TABLET; ORAL
Proprietary Name : BUTABARBITAL SODIUM
Dosage Strength : 16.2MG
Approval Date : 1982-01-01
Application Number : 83606
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Solvay Chemicals International S.A
Dosage Form : TABLET; ORAL
Proprietary Name : BUTABARBITAL SODIUM
Dosage Strength : 97.2MG
Approval Date : 1982-01-01
Application Number : 83896
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Solvay Chemicals International S.A
Dosage Form : TABLET; ORAL
Proprietary Name : BUTABARBITAL SODIUM
Dosage Strength : 48.6MG
Approval Date : 1982-01-01
Application Number : 83897
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Solvay Chemicals International S.A
Dosage Form : TABLET; ORAL
Proprietary Name : BUTABARBITAL SODIUM
Dosage Strength : 32.4MG
Approval Date : 1982-01-01
Application Number : 83898
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Solvay Chemicals International S.A
Dosage Form : TABLET; ORAL
Proprietary Name : DEXONE 1.5
Dosage Strength : 1.5MG
Approval Date : 1982-01-01
Application Number : 84990
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Solvay Chemicals International S.A
Dosage Form : TABLET; ORAL
Proprietary Name : DEXONE 0.5
Dosage Strength : 0.5MG
Approval Date : 1982-01-01
Application Number : 84991
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Solvay Chemicals International S.a is a supplier offers 14 products (APIs, Excipients or Intermediates).
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