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Haloperidol Decanoate
Haloperidol Decanoate - 0703-7021-03 - (Haloperidol Decanoate)
Drug Information of Haloperidol Decanoate
| Product NDC: | 0703-7021 |
| Proprietary Name: | Haloperidol Decanoate |
| Non Proprietary Name: | Haloperidol Decanoate |
| Active Ingredient(s): | 100 mg/mL & nbsp; Haloperidol Decanoate |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Haloperidol Decanoate
| Product NDC: | 0703-7021 |
| Labeler Name: | Teva Parenteral Medicines, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075393 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990604 |
Package Information of Haloperidol Decanoate
| Package NDC: | 0703-7021-03 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 CARTON (0703-7021-03) > 1 mL in 1 VIAL, SINGLE-DOSE (0703-7021-01) |
NDC Information of Haloperidol Decanoate
| NDC Code | 0703-7021-03 |
| Proprietary Name | Haloperidol Decanoate |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (0703-7021-03) > 1 mL in 1 VIAL, SINGLE-DOSE (0703-7021-01) |
| Product NDC | 0703-7021 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Haloperidol Decanoate |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 19990604 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc. |
| Substance Name | HALOPERIDOL DECANOATE |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Typical Antipsychotic [EPC] |
