Phendimetrazine Tartrate
- Product NDC
- 68071-3062
- 11-digit product format
- 680713062
- Labeler code
- 68071
- Product ID
- 68071-3062_bb12cdd1-6170-b57d-e053-2a95a90ac21e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phendimetrazine Tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA085588
- Marketing category
- ANDA
- Marketing start
- 1997-08-19
- 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-3062-3 | 68071306203 | 30 TABLET in 1 BOTTLE (68071-3062-3) | 30 tablet | 2017-03-10 | 0000-00-00 | No | No | Current |
| 68071-3062-6 | 68071306206 | 60 TABLET in 1 BOTTLE (68071-3062-6) | 60 tablet | 2017-03-10 | 0000-00-00 | No | No | Current |
| 68071-3062-9 | 68071306209 | 90 TABLET in 1 BOTTLE (68071-3062-9) | 90 tablet | 2017-03-10 | 0000-00-00 | No | No | Current |