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Cyclopentolate Hydrochloride
Cyclopentolate Hydrochloride - 61314-397-01 - (Cyclopentolate Hydrochloride)
Drug Information of Cyclopentolate Hydrochloride
| Product NDC: | 61314-397 |
| Proprietary Name: | Cyclopentolate Hydrochloride |
| Non Proprietary Name: | Cyclopentolate Hydrochloride |
| Active Ingredient(s): | 20 mg/mL & nbsp; Cyclopentolate Hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cyclopentolate Hydrochloride
| Product NDC: | 61314-397 |
| Labeler Name: | Falcon Pharmaceuticals, Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA084108 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020822 |
Package Information of Cyclopentolate Hydrochloride
| Package NDC: | 61314-397-01 |
| Package Description: | 2 mL in 1 BOTTLE (61314-397-01) |
NDC Information of Cyclopentolate Hydrochloride
| NDC Code | 61314-397-01 |
| Proprietary Name | Cyclopentolate Hydrochloride |
| Package Description | 2 mL in 1 BOTTLE (61314-397-01) |
| Product NDC | 61314-397 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cyclopentolate Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20020822 |
| Marketing Category Name | ANDA |
| Labeler Name | Falcon Pharmaceuticals, Ltd. |
| Substance Name | CYCLOPENTOLATE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
