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Phenylephrine
Phenylephrine - 21695-524-18 - (Phenylephrine)
Drug Information of Phenylephrine
| Product NDC: | 21695-524 |
| Proprietary Name: | Phenylephrine |
| Non Proprietary Name: | Phenylephrine |
| Active Ingredient(s): | 10 mg/1 & nbsp; Phenylephrine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phenylephrine
| Product NDC: | 21695-524 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100224 |
Package Information of Phenylephrine
| Package NDC: | 21695-524-18 |
| Package Description: | 18 TABLET in 1 BLISTER PACK (21695-524-18) |
NDC Information of Phenylephrine
| NDC Code | 21695-524-18 |
| Proprietary Name | Phenylephrine |
| Package Description | 18 TABLET in 1 BLISTER PACK (21695-524-18) |
| Product NDC | 21695-524 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Phenylephrine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100224 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
