phentermine hydrochloride
- Product NDC
- 50436-9028
- 11-digit product format
- 504369028
- Labeler code
- 50436
- Product ID
- 50436-9028_d761706f-1f5b-4f11-be5c-7e88eb360fa9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- phentermine hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA087190
- Marketing category
- ANDA
- Marketing start
- 1981-06-12
- Marketing end
- 0000-00-00
- Substance
- PHENTERMINE HYDROCHLORIDE
- Active strength
- 30 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