Cyclopentolate
- Product NDC
- 17478-096
- 11-digit product format
- 174780096
- Labeler code
- 17478
- Product ID
- 17478-096_55516550-81ea-4aab-aea4-0e1351c478bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclopentolate Hydrochloride
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Akorn
- Application
- ANDA205937
- Marketing category
- ANDA
- Marketing start
- 2015-12-10
- Marketing end
- 0000-00-00
- Substance
- CYCLOPENTOLATE HYDROCHLORIDE
- Active strength
- 5 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17478-096-15 | Cyclopentolate | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 5 |
| 17478-096-15 | Cyclopentolate | 15 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 15 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17478-096 | CYCLOPENTOLATE (CYCLOPENTOLATE HYDROCHLORIDE) SOLUTION/ DROPS [AKORN] | 5 | Legacy NDC, 2 package rows | 20220126_84a02489-2753-4543-9712-0345074e5972.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-096-15 | 17478009615 | 1 BOTTLE, DROPPER in 1 CARTON (17478-096-15) > 15 mL in 1 BOTTLE, DROPPER | 2015-12-10 | 0000-00-00 | No | No | Current |