01 2ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE
02 1DOXYLAMINE SUCCINATE
03 12FEXOFENADINE HYDROCHLORIDE
04 2FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
05 4LEVOCETIRIZINE DIHYDROCHLORIDE
06 3NICOTINE
07 4RANITIDINE HYDROCHLORIDE
08 1SELENIUM SULFIDE
09 2TRIAMCINOLONE ACETONIDE
01 2CHATTEM
02 29CHATTEM SANOFI
01 1AEROSOL, METERED;NASAL
02 1CAPSULE;ORAL
03 3FILM, EXTENDED RELEASE;TRANSDERMAL
04 1LOTION/SHAMPOO;TOPICAL
05 2SOLUTION;ORAL
06 1SPRAY, METERED;NASAL
07 3SUSPENSION;ORAL
08 2TABLET, CHEWABLE;ORAL
09 1TABLET, EFFERVESCENT;ORAL
10 2TABLET, EXTENDED RELEASE;ORAL
11 2TABLET, ORALLY DISINTEGRATING;ORAL
12 12TABLET;ORAL
01 10.055MG/INH
02 10.055MG/SPRAY
03 114MG/24HR
04 1160MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
05 2180MG
06 1180MG;240MG
07 12.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 12.5MG/5ML
09 12.5MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
10 121MG/24HR
11 125MG
12 230MG
13 230MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
14 230MG/5ML
15 130MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
16 15MG
17 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
18 260MG
19 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 160MG;120MG
21 17MG/24HR
22 180MG;20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 2EQ 150MG BASE
24 1EQ 75MG BASE
25 1EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
01 31USA
Regulatory Info : DISCN
Registration Country : USA
ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE
Dosage Form : TABLET, CHEWABLE;ORAL
Brand Name : GAVISCON
Dosage Strength : 80MG;20MG **Federal Re...
Packaging :
Approval Date : 1983-12-09
Application Number : 18685
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE
Dosage Form : TABLET, CHEWABLE;ORAL
Brand Name : GAVISCON
Dosage Strength : 160MG;40MG **Federal R...
Packaging :
Approval Date : 1983-12-09
Application Number : 18685
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : UNISOM
Dosage Strength : 25MG
Packaging :
Approval Date : 1982-01-01
Application Number : 18066
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : CHILDRENS ALLEGRA ALLERGY
Dosage Strength : 30MG **Federal Registe...
Packaging :
Approval Date : 2011-01-24
Application Number : 20872
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : CHILDRENS ALLEGRA HIVES
Dosage Strength : 30MG
Packaging :
Approval Date : 2011-01-24
Application Number : 20872
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ALLEGRA HIVES
Dosage Strength : 60MG
Packaging :
Approval Date : 2011-01-24
Application Number : 20872
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ALLEGRA HIVES
Dosage Strength : 180MG
Packaging :
Approval Date : 2011-01-24
Application Number : 20872
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET, ORALLY DISINTEGR...
Brand Name : CHILDRENS ALLEGRA ALLERGY
Dosage Strength : 30MG
Packaging :
Approval Date : 2011-01-24
Application Number : 21909
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SUSPENSION;ORAL
Brand Name : ALLEGRA
Dosage Strength : 30MG/5ML
Packaging :
Approval Date : 2006-10-16
Application Number : 21963
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Dosage Form : SUSPENSION;ORAL
Brand Name : CHILDRENS ALLEGRA ALLERGY
Dosage Strength : 30MG/5ML
Packaging :
Approval Date : 2011-01-24
Application Number : 201373
Regulatory Info : OTC
Registration Country : USA
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