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SINE OFF
SINE OFF - 51645-291-24 - (ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE)
Drug Information of SINE OFF
| Product NDC: | 51645-291 |
| Proprietary Name: | SINE OFF |
| Non Proprietary Name: | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient(s): | 500; 2; 5 mg/1; mg/1; mg/1 & nbsp; ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SINE OFF
| Product NDC: | 51645-291 |
| Labeler Name: | Gemini Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100705 |
Package Information of SINE OFF
| Package NDC: | 51645-291-24 |
| Package Description: | 2 BLISTER PACK in 1 BOX (51645-291-24) > 12 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of SINE OFF
| NDC Code | 51645-291-24 |
| Proprietary Name | SINE OFF |
| Package Description | 2 BLISTER PACK in 1 BOX (51645-291-24) > 12 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 51645-291 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100705 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Gemini Pharmaceuticals, Inc. |
| Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 500; 2; 5 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
