phendimetrazine tartrate
- Product NDC
- 0463-8500
- 11-digit product format
- 004638500
- Labeler code
- 0463
- Product ID
- 0463-8500_7b09c11c-9ccf-0ec9-e053-2991aa0a39b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- phendimetrazine tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- C.O. Truxton, Inc.
- Application
- ANDA089452
- Marketing category
- ANDA
- Marketing start
- 2001-07-26
- Marketing end
- 2020-01-12
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record