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Nasal Decongestant PE
Nasal Decongestant PE - 30142-670-36 - (Phenylephrine Hydrochloride)
Drug Information of Nasal Decongestant PE
| Product NDC: | 30142-670 |
| Proprietary Name: | Nasal Decongestant PE |
| Non Proprietary Name: | Phenylephrine Hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nasal Decongestant PE
| Product NDC: | 30142-670 |
| Labeler Name: | The Kroger Co. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110202 |
Package Information of Nasal Decongestant PE
| Package NDC: | 30142-670-36 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (30142-670-36) > 18 TABLET in 1 BLISTER PACK |
NDC Information of Nasal Decongestant PE
| NDC Code | 30142-670-36 |
| Proprietary Name | Nasal Decongestant PE |
| Package Description | 2 BLISTER PACK in 1 CARTON (30142-670-36) > 18 TABLET in 1 BLISTER PACK |
| Product NDC | 30142-670 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Phenylephrine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110202 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Kroger Co. |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
