fluphenazine hydrochloride
- Product NDC
- 60219-1679
- 11-digit product format
- 602191679
- Labeler code
- 60219
- Product ID
- 60219-1679_2933569f-f526-47a0-a925-994e0c70ce2d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fluphenazine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals NY LLC
- Application
- ANDA213647
- Marketing category
- ANDA
- Marketing start
- 2020-07-11
- Marketing end
- 0000-00-00
- Substance
- FLUPHENAZINE HYDROCHLORIDE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Phenothiazines [CS],Phenothiazine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 60219-1679-1 | fluphenazine hydrochloride | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60219-1679 | FLUPHENAZINE HYDROCHLORIDE TABLET, FILM COATED [AMNEAL PHARMACEUTICALS NY LLC] | 7 | Legacy NDC, 1 package rows | 20201105_4ad994f7-0caf-40aa-8824-ff438f7fc366.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60219-1679-1 | 60219167901 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60219-1679-1) | 2020-07-11 | 0000-00-00 | No | No | Current |