Phentermine Hydrochloride
- Product NDC
- 50090-1114
- 11-digit product format
- 500901114
- Labeler code
- 50090
- Product ID
- 50090-1114_28f00a47-dc28-47e9-a318-3a80bafd1fd3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions LLC
- Application
- ANDA040526
- Marketing category
- ANDA
- Marketing start
- 2013-08-12
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#