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Cyclopentolate Hydrochloride
Cyclopentolate Hydrochloride - 17478-097-02 - (Cyclopentolate Hydrochloride)
Drug Information of Cyclopentolate Hydrochloride
| Product NDC: | 17478-097 |
| 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/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cyclopentolate Hydrochloride
| Product NDC: | 17478-097 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040165 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19970113 |
Package Information of Cyclopentolate Hydrochloride
| Package NDC: | 17478-097-02 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (17478-097-02) > 2 mL in 1 BOTTLE, DROPPER |
NDC Information of Cyclopentolate Hydrochloride
| NDC Code | 17478-097-02 |
| Proprietary Name | Cyclopentolate Hydrochloride |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (17478-097-02) > 2 mL in 1 BOTTLE, DROPPER |
| Product NDC | 17478-097 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cyclopentolate Hydrochloride |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19970113 |
| Marketing Category Name | ANDA |
| Labeler Name | Akorn, Inc. |
| Substance Name | CYCLOPENTOLATE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
