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Night Time Sinus
Night Time Sinus - 55315-102-16 - (Acetaminophen, Doxylamine Succinate, Phenylephrine Hydrochloride)
Drug Information of Night Time Sinus
| Product NDC: | 55315-102 |
| Proprietary Name: | Night Time Sinus |
| Non Proprietary Name: | Acetaminophen, Doxylamine Succinate, Phenylephrine Hydrochloride |
| Active Ingredient(s): | 325; 6.25; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Doxylamine Succinate, Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Night Time Sinus
| Product NDC: | 55315-102 |
| Labeler Name: | Freds, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121205 |
Package Information of Night Time Sinus
| Package NDC: | 55315-102-16 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (55315-102-16) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Information of Night Time Sinus
| NDC Code | 55315-102-16 |
| Proprietary Name | Night Time Sinus |
| Package Description | 1 BLISTER PACK in 1 CARTON (55315-102-16) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| Product NDC | 55315-102 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Doxylamine Succinate, Phenylephrine Hydrochloride |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20121205 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Freds, Inc. |
| Substance Name | ACETAMINOPHEN; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 6.25; 5 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
