Paroxetine
- Product NDC
- 21695-101
- 11-digit product format
- 216950101
- Labeler code
- 21695
- Product ID
- 21695-101_0d4fb45b-e45b-4519-96a3-a8a106450f87
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Paroxetine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA077584
- Marketing category
- ANDA
- Marketing start
- 2007-04-13
- Marketing end
- 0000-00-00
- Substance
- PAROXETINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 21695-101-30 | Paroxetine | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
| 21695-101-60 | Paroxetine | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 1 |
| 21695-101-90 | Paroxetine | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-101 | PAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 3 package rows | 20110113_0d4fb45b-e45b-4519-96a3-a8a106450f87.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-101-30 | 21695010130 | 30 in 1 BOTTLE | Historical |
| 21695-101-60 | 21695010160 | 60 in 1 BOTTLE | Historical |
| 21695-101-90 | 21695010190 | 90 in 1 BOTTLE | Historical |