Cyclopentolate Hydrochloride
- Product NDC
- 50090-3234
- 11-digit product format
- 500903234
- Labeler code
- 50090
- Product ID
- 50090-3234_d6cc3909-4044-4488-a9fe-5294f7bcbc98
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclopentolate Hydrochloride
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- A-S Medication Solutions
- Application
- ANDA084110
- Marketing category
- ANDA
- Marketing start
- 2002-08-22
- Marketing end
- 0000-00-00
- Substance
- CYCLOPENTOLATE HYDROCHLORIDE
- Active strength
- 10 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 50090-3234-1 | Cyclopentolate Hydrochloride | 15 mL in 1 BOTTLE | SOLUTION | 15 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3234 | CYCLOPENTOLATE HYDROCHLORIDE SOLUTION [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 1 package rows | 20200122_18db4e54-68f4-4711-b087-0a89df4edc1d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3234-1 | 50090323401 | 15 mL in 1 BOTTLE (50090-3234-1) | 15 ml | 2017-11-01 | 0000-00-00 | No | No | Current |