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DIPHENDYDRAMINE HYDROCHLORIDE
DIPHENDYDRAMINE HYDROCHLORIDE - 24236-200-02 - (DIPHENDYDRAMINE HYDROCHLORIDE)
Drug Information of DIPHENDYDRAMINE HYDROCHLORIDE
| Product NDC: | 24236-200 |
| Proprietary Name: | DIPHENDYDRAMINE HYDROCHLORIDE |
| Non Proprietary Name: | DIPHENDYDRAMINE HYDROCHLORIDE |
| Active Ingredient(s): | 25 mg/1 & nbsp; DIPHENDYDRAMINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DIPHENDYDRAMINE HYDROCHLORIDE
| Product NDC: | 24236-200 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075659 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101217 |
Package Information of DIPHENDYDRAMINE HYDROCHLORIDE
| Package NDC: | 24236-200-02 |
| Package Description: | 30 CAPSULE in 1 BLISTER PACK (24236-200-02) |
NDC Information of DIPHENDYDRAMINE HYDROCHLORIDE
| NDC Code | 24236-200-02 |
| Proprietary Name | DIPHENDYDRAMINE HYDROCHLORIDE |
| Package Description | 30 CAPSULE in 1 BLISTER PACK (24236-200-02) |
| Product NDC | 24236-200 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DIPHENDYDRAMINE HYDROCHLORIDE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20101217 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
