Cyproheptadine Hydrochloride
- Product NDC
- 69367-246
- 11-digit product format
- 693670246
- Labeler code
- 69367
- Product ID
- 69367-246_b5c541ec-cd1b-42d8-a3fb-cd4adb2cf2cf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyproheptadine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Westminster Pharmaceuticals, LLC
- Application
- ANDA207555
- Marketing category
- ANDA
- Marketing start
- 2020-01-06
- 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 |
|---|
| 69367-246 | CYPROHEPTADINE HYDROCHLORIDE TABLET [WESTMINSTER PHARMACEUTICALS, LLC] | 3 | Legacy NDC | 20241215_526654c3-4c79-467e-ac73-01ae84ddbd78.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69367-246-01 | 69367024601 | 100 TABLET in 1 BOTTLE, PLASTIC (69367-246-01) | 100 tablet | 2020-01-06 | 0000-00-00 | No | No | Current |
| 69367-246-10 | 69367024610 | 1000 TABLET in 1 BOTTLE, PLASTIC (69367-246-10) | 1000 tablet | 2020-01-06 | 0000-00-00 | No | No | Current |