Phentermine Hydrochloride
- Product NDC
- 68788-7502
- 11-digit product format
- 687887502
- Labeler code
- 68788
- Product ID
- 68788-7502_b4bcc34c-0814-4084-8bc7-6cd5b5d57ca5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA202248
- Marketing category
- ANDA
- Marketing start
- 2012-02-17
- 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
- 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 |
|---|
| 68788-7502-1 | 68788750201 | 7 CAPSULE in 1 BOTTLE (68788-7502-1) | 7 capsule | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7502-3 | 68788750203 | 30 CAPSULE in 1 BOTTLE (68788-7502-3) | 30 capsule | 2019-12-27 | 0000-00-00 | No | No | Current |