Phentermine Hydrochloride
- Product NDC
- 68788-7823
- 11-digit product format
- 687887823
- Labeler code
- 68788
- Product ID
- 68788-7823_b51c120a-4028-4804-b0a3-d64f3d81d8ef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA040876
- Marketing category
- ANDA
- Marketing start
- 2020-11-20
- 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
- 2022-12-31
- 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 |
|---|
| 68788-7823-1 | 68788782301 | 7 TABLET in 1 BOTTLE (68788-7823-1) | 7 tablet | 2020-11-20 | 0000-00-00 | No | No | Current |
| 68788-7823-3 | 68788782303 | 30 TABLET in 1 BOTTLE (68788-7823-3) | 30 tablet | 2020-11-20 | 0000-00-00 | No | No | Current |
| 68788-7823-5 | 68788782305 | 15 TABLET in 1 BOTTLE (68788-7823-5) | 15 tablet | 2020-11-20 | 0000-00-00 | No | No | Current |