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CITRUCEL
CITRUCEL - 0135-0199-02 - (methylcellulose)
Drug Information of CITRUCEL
| Product NDC: | 0135-0199 |
| Proprietary Name: | CITRUCEL |
| Non Proprietary Name: | methylcellulose |
| Active Ingredient(s): | 500 mg/1 & nbsp; methylcellulose |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CITRUCEL
| Product NDC: | 0135-0199 |
| Labeler Name: | GlaxoSmithKline Consumer Healthcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100201 |
Package Information of CITRUCEL
| Package NDC: | 0135-0199-02 |
| Package Description: | 100 TABLET in 1 BOTTLE (0135-0199-02) |
NDC Information of CITRUCEL
| NDC Code | 0135-0199-02 |
| Proprietary Name | CITRUCEL |
| Package Description | 100 TABLET in 1 BOTTLE (0135-0199-02) |
| Product NDC | 0135-0199 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | methylcellulose |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | GlaxoSmithKline Consumer Healthcare LP |
| Substance Name | METHYLCELLULOSE (4000 MPA.S) |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
