Phendimetrazine Tartrate
- Product NDC
- 17224-500
- 11-digit product format
- 172240500
- Labeler code
- 17224
- Product ID
- 17224-500_b8690e43-bc8d-487f-b9ec-5c786ecbe824
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phendimetrazine Tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- CALVIN, SCOTT AND COMPANY, INCORPORATED
- Application
- ANDA091042
- Marketing category
- ANDA
- Marketing start
- 2010-09-15
- 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
- 2020-12-31
- 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 |
|---|
| 17224-500-10 | Phendimetrazine Tartrate | 28 in 1 BOTTLE | TABLET | 28 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17224-500 | PHENDIMETRAZINE TARTRATE TABLET [CALVIN, SCOTT AND COMPANY, INCORPORATED] | 3 | Legacy NDC, 1 package rows | 20191120_f279e3a1-46ef-458e-9587-16b09e72a991.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 17224-500-10 | 17224050010 | 28 in 1 BOTTLE | Historical |