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Loperamide Hydrochloride
Loperamide Hydrochloride - 51079-690-19 - (loperamide hydrochloride)
Drug Information of Loperamide Hydrochloride
| Product NDC: | 51079-690 |
| Proprietary Name: | Loperamide Hydrochloride |
| Non Proprietary Name: | loperamide hydrochloride |
| Active Ingredient(s): | 2 mg/1 & nbsp; loperamide hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Loperamide Hydrochloride
| Product NDC: | 51079-690 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072741 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110727 |
Package Information of Loperamide Hydrochloride
| Package NDC: | 51079-690-19 |
| Package Description: | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-690-19) > 1 CAPSULE in 1 BLISTER PACK (51079-690-17) |
NDC Information of Loperamide Hydrochloride
| NDC Code | 51079-690-19 |
| Proprietary Name | Loperamide Hydrochloride |
| Package Description | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-690-19) > 1 CAPSULE in 1 BLISTER PACK (51079-690-17) |
| Product NDC | 51079-690 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | loperamide hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20110727 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | LOPERAMIDE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
