Cyproheptadine Hydrochloride
- Product NDC
- 71205-024
- 11-digit product format
- 712050024
- Labeler code
- 71205
- Product ID
- 71205-024_5914f311-a4d5-4388-8939-d53eb183e612
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyproheptadine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA207783
- Marketing category
- ANDA
- Marketing start
- 2017-02-21
- Marketing end
- 0000-00-00
- Substance
- CYPROHEPTADINE HYDROCHLORIDE
- Active strength
- 4 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-024 | CYPROHEPTADINE HYDROCHLORIDE TABLET [PROFICIENT RX LP] | 3 | Legacy NDC | 20191101_1a848398-107c-4075-ba19-59369df135a8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-024-30 | 71205002430 | 30 TABLET in 1 BOTTLE, PLASTIC (71205-024-30) | 30 tablet | 2018-05-01 | 0000-00-00 | No | No | Current |
| 71205-024-60 | 71205002460 | 60 TABLET in 1 BOTTLE, PLASTIC (71205-024-60) | 60 tablet | 2018-05-01 | 0000-00-00 | No | No | Current |
| 71205-024-90 | 71205002490 | 90 TABLET in 1 BOTTLE, PLASTIC (71205-024-90) | 90 tablet | 2018-05-01 | 0000-00-00 | No | No | Current |