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Haloperidol
Haloperidol - 76237-260-30 - (haloperidol)
Drug Information of Haloperidol
| Product NDC: | 76237-260 |
| Proprietary Name: | Haloperidol |
| Non Proprietary Name: | haloperidol |
| Active Ingredient(s): | 5 mg/1 & nbsp; haloperidol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Haloperidol
| Product NDC: | 76237-260 |
| Labeler Name: | McKesson Contract Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070278 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130410 |
Package Information of Haloperidol
| Package NDC: | 76237-260-30 |
| Package Description: | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-260-30) > 5 TABLET in 1 BLISTER PACK |
NDC Information of Haloperidol
| NDC Code | 76237-260-30 |
| Proprietary Name | Haloperidol |
| Package Description | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-260-30) > 5 TABLET in 1 BLISTER PACK |
| Product NDC | 76237-260 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | haloperidol |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130410 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Contract Packaging |
| Substance Name | HALOPERIDOL |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Typical Antipsychotic [EPC] |
