Phentermine Hydrochloride
- Product NDC
- 50436-6743
- 11-digit product format
- 504366743
- Labeler code
- 50436
- Product ID
- 50436-6743_0cfd103d-4e9d-4555-bcaf-d2d24a48adf4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA040887
- Marketing category
- ANDA
- Marketing start
- 2012-08-15
- Marketing end
- 0000-00-00
- Substance
- PHENTERMINE HYDROCHLORIDE
- Active strength
- 38 mg/1
- Pharmacologic classes
- Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record