PHENDIMETRAZINE TARTRATE
- Product NDC
- 68071-2605
- 11-digit product format
- 680712605
- Labeler code
- 68071
- Product ID
- 68071-2605_dca5f584-a826-47f7-e053-2995a90a4b68
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PHENDIMETRAZINE TARTRATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA085588
- Marketing category
- ANDA
- Marketing start
- 2018-07-01
- Marketing end
- 0000-00-00
- Substance
- PHENDIMETRAZINE TARTRATE
- Active strength
- 35 mg/1
- Pharmacologic classes
- Appetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 68071-2605-9 | PHENDIMETRAZINE TARTRATE | 90 in 1 BOTTLE | TABLET | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2605 | PHENDIMETRAZINE TARTRATE TABLET [NUCARE PHARMACEUTICALS,INC.] | 4 | Legacy NDC, 1 package rows | 20230715_d3c58ccf-0099-ed13-e053-2a95a90a4daa.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2605-3 | 68071260503 | 30 TABLET in 1 BOTTLE (68071-2605-3) | 30 tablet | 2021-12-22 | 0000-00-00 | No | No | Current |
| 68071-2605-6 | 68071260506 | 60 TABLET in 1 BOTTLE (68071-2605-6) | 60 tablet | 2021-12-22 | 0000-00-00 | No | No | Current |
| 68071-2605-9 | 68071260509 | 90 TABLET in 1 BOTTLE (68071-2605-9) | 90 tablet | 2021-12-22 | 0000-00-00 | No | No | Current |