GLUCOSAMINE SULFATE, CHONDROITIN SULFATE, IBUPROFEN
glucosamine sulfate, chondroitin sulfate, ibuprofen capsule |
Product Information |
Product Type | HUMAN OTC DRUG | Item Code (Source) | NDC: 10267-3479 |
Route of Administration | ORAL |
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Active Ingredient/Active Moiety |
Ingredient Name | Basis of Strength | Strength |
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) (GLUCOSAMINE - UNII:N08U5BOQ1K) | GLUCOSAMINE SULFATE | 250 mg |
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) | IBUPROFEN | 100 mg |
CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z) (CONDOLIASE - UNII:7SI2UZG934) | CHONDROITIN SULFATE (BOVINE) | 200 mg |
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Product Characteristics |
Color | white (blue) | Score | no score |
Shape | CAPSULE | Size | 22mm |
Flavor | | Imprint Code |
THERAFLEX;ADVANCE
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Contains | |
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Packaging |
# | Item Code | Package Description | Marketing Start Date | Marketing End Date |
1 | NDC: 10267-3479-3 | 1 in 1 CARTON | 05/24/2011 | |
1 | | 30 in 1 BOTTLE; Type 0: Not a Combination Product | | |
2 | NDC: 10267-3479-7 | 1 in 1 CARTON | 04/19/2010 | |
2 | | 60 in 1 BOTTLE; Type 0: Not a Combination Product | | |
3 | NDC: 10267-3479-5 | 1 in 1 CARTON | 04/19/2010 | |
3 | | 120 in 1 BOTTLE; Type 0: Not a Combination Product | | |
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Marketing Information |
Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
Export only | | 04/19/2010 | |
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