Cyproheptadine Hydrochloride
- Product NDC
- 68151-1728
- 11-digit product format
- 681511728
- Labeler code
- 68151
- Product ID
- 68151-1728_20f392a7-158d-4507-b054-c309642a4bc9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyproheptadine Hydrochloride
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA040668
- Marketing category
- ANDA
- Marketing start
- 2006-07-10
- Marketing end
- 0000-00-00
- Substance
- CYPROHEPTADINE HYDROCHLORIDE
- Active strength
- 2 mg/5mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 68151-1728-7 | Cyproheptadine Hydrochloride | 1 mL in 1 BOTTLE | SYRUP | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-1728 | CYPROHEPTADINE HYDROCHLORIDE SYRUP [CARILION MATERIALS MANAGEMENT] | 2 | Legacy NDC, 1 package rows | 20160213_949743a7-f922-4248-aa28-818236c80a67.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 68151-1728-7 | 68151172807 | 1 mL in 1 BOTTLE | 1 ml | Historical |