PHENDIMETRAZINE TARTRATE
- Product NDC
- 68462-561
- 11-digit product format
- 684620561
- Labeler code
- 68462
- Product ID
- 68462-561_8857fb11-5458-4629-b91c-7dfccebcfcb4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phendimetrazine Tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Glenmark Pharmaceuticals Inc.,USA
- Application
- ANDA040762
- Marketing category
- ANDA
- Marketing start
- 2012-11-20
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68462-561-01 | 68462056101 | 100 TABLET in 1 BOTTLE (68462-561-01) | 100 tablet | 2018-08-31 | 0000-00-00 | No | No | Current |
| 68462-561-10 | 68462056110 | 1000 TABLET in 1 BOTTLE (68462-561-10) | 1000 tablet | 2018-08-31 | 0000-00-00 | No | No | Current |