phentermine hydrochloride
- Product NDC
- 0185-5000
- 11-digit product format
- 001855000
- Labeler code
- 0185
- Product ID
- 0185-5000_8c3c3331-2016-4a0c-93b3-7198ca1d029e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- phentermine hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Eon Labs, Inc.
- Application
- ANDA086945
- Marketing category
- ANDA
- Marketing start
- 1983-07-20
- Marketing end
- 2023-08-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0185-5000-01 | 00185500001 | 100 CAPSULE in 1 BOTTLE (0185-5000-01) | 100 capsule | 1983-07-20 | 2023-08-31 | No | No | Current |
| 0185-5000-10 | 00185500010 | 1000 CAPSULE in 1 BOTTLE (0185-5000-10) | 1000 capsule | 1983-07-20 | 2023-05-31 | No | No | Current |