Phendimetrazine
- Product NDC
- 51655-005
- 11-digit product format
- 516550005
- Labeler code
- 51655
- Product ID
- 51655-005_d47916f4-096d-d02e-e053-2a95a90a1129
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phendimetrazine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals
- Application
- ANDA091042
- Marketing category
- ANDA
- Marketing start
- 2015-04-22
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-005 | PHENDIMETRAZINE TABLET [NORTHWIND PHARMACEUTICALS] | 4 | Legacy NDC | 20220101_4a64fde2-1db7-5878-e054-00144ff8d46c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51655-005-52 | 51655000552 | 30 TABLET in 1 BOTTLE (51655-005-52) | 30 tablet | 2015-04-22 | 0000-00-00 | No | No | Current |