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SINE OFF
SINE OFF - 51645-269-12 - (ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE)
Drug Information of SINE OFF
| Product NDC: | 51645-269 |
| Proprietary Name: | SINE OFF |
| Non Proprietary Name: | ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient(s): | 500; 5 mg/1; mg/1 & nbsp; ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SINE OFF
| Product NDC: | 51645-269 |
| Labeler Name: | Gemini Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100705 |
Package Information of SINE OFF
| Package NDC: | 51645-269-12 |
| Package Description: | 1 BLISTER PACK in 1 BOX (51645-269-12) > 12 TABLET, COATED in 1 BLISTER PACK |
NDC Information of SINE OFF
| NDC Code | 51645-269-12 |
| Proprietary Name | SINE OFF |
| Package Description | 1 BLISTER PACK in 1 BOX (51645-269-12) > 12 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 51645-269 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100705 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Gemini Pharmaceuticals, Inc. |
| Substance Name | ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 500; 5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
