Paroxetine
- Product NDC
- 60760-501
- 11-digit product format
- 607600501
- Labeler code
- 60760
- Product ID
- 60760-501_850242ce-1785-a974-e053-2991aa0a4387
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Paroxetine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA077584
- Marketing category
- ANDA
- Marketing start
- 2019-03-20
- Marketing end
- 0000-00-00
- Substance
- PAROXETINE HYDROCHLORIDE HEMIHYDRATE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- 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 |
|---|
| 60760-501 | PAROXETINE TABLET, FILM COATED [ST. MARY'S MEDICAL PARK PHARMACY] | 1 | Legacy NDC | 20190329_85020e9f-cff1-8327-e053-2a91aa0abc38.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-501-90 | 60760050190 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-501-90) | 2019-03-20 | 0000-00-00 | No | No | Current |