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Allergy Antihistamine
Allergy Antihistamine - 52904-460-02 - (Diphenhydramine Hydrochloride)
Drug Information of Allergy Antihistamine
| Product NDC: | 52904-460 |
| Proprietary Name: | Allergy Antihistamine |
| Non Proprietary Name: | Diphenhydramine Hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; Diphenhydramine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Allergy Antihistamine
| Product NDC: | 52904-460 |
| Labeler Name: | Select Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121015 |
Package Information of Allergy Antihistamine
| Package NDC: | 52904-460-02 |
| Package Description: | 2 TABLET in 1 PACKET (52904-460-02) |
NDC Information of Allergy Antihistamine
| NDC Code | 52904-460-02 |
| Proprietary Name | Allergy Antihistamine |
| Package Description | 2 TABLET in 1 PACKET (52904-460-02) |
| Product NDC | 52904-460 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121015 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Select Corporation |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
