GLUCOSAMINE SULFATE, CHONDROITIN SULFATE, IBUPROFEN capsule

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z) (CONDOLIASE - UNII:7SI2UZG934), GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) (GLUCOSAMINE - UNII:N08U5BOQ1K), IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM)

Available from:

Contract Pharmacal Corp.

Administration route:

ORAL

Prescription type:

OTC DRUG

Authorization status:

Export only

Summary of Product characteristics

GLUCOSAMINE SULFATE, CHONDROITIN SULFATE, IBUPROFEN- GLUCOSAMINE
SULFATE, CHONDROITIN SULFATE, IBUPROFEN CAPSULE
CONTRACT PHARMACAL CORP.
----------
3479- EXPORT
BELARUS LABEL
RUSSIA LABEL
KAZAKHASTAN LABEL
UKRAINE LABEL
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
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z) (CONDOLIASE -
UNII:7SI2UZ G934)
CHONDROITIN SULFATE
(BOVINE)
200 mg
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) (GLUCOSAMINE -
UNII:N08U5BOQ1K)
GLUCOSAMINE SULFATE
250 mg
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM)
IBUPROFEN
100 mg
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
STARCH, CORN (UNII: O8232NY3SJ)
CROSPOVIDONE (UNII: 2S7830E561)
STEARIC ACID (UNII: 4ELV7Z65AP)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
MAGNESIUM STEARATE (UNII: 70097M6I30)
GELATIN (UNII: 2G86QN327L)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
POVIDONE K30 (UNII: U725QWY32X)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
PRODUCT CHARACTERISTICS
COLOR
white (blue)
SCORE
no score
SHAPE
CAPSULE
SIZE
22mm
FLAVOR
IMPRINT CODE
THERAFLEX;ADVANCE
CONTAINS
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:10267-
3479-3
1 in 1 CARTON
05/24/2011
09/30/2018
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
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETING END
DATE
Export only
04/19/2010
Contract Pharmacal Corp.
LABELER -
Contract Pharmacal Corp. (057795122)
Revised: 4/2023