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Dicyclomine Hydrochloride
Dicyclomine Hydrochloride - 51079-119-20 - (Dicyclomine Hydrochloride)
Drug Information of Dicyclomine Hydrochloride
| Product NDC: | 51079-119 |
| Proprietary Name: | Dicyclomine Hydrochloride |
| Non Proprietary Name: | Dicyclomine Hydrochloride |
| Active Ingredient(s): | 20 mg/1 & nbsp; Dicyclomine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dicyclomine Hydrochloride
| Product NDC: | 51079-119 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040317 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110816 |
Package Information of Dicyclomine Hydrochloride
| Package NDC: | 51079-119-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-119-20) > 1 TABLET in 1 BLISTER PACK (51079-119-01) |
NDC Information of Dicyclomine Hydrochloride
| NDC Code | 51079-119-20 |
| Proprietary Name | Dicyclomine Hydrochloride |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-119-20) > 1 TABLET in 1 BLISTER PACK (51079-119-01) |
| Product NDC | 51079-119 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dicyclomine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110816 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | DICYCLOMINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
