Phentermine Hydrochloride
- Product NDC
- 68071-3241
- 11-digit product format
- 680713241
- Labeler code
- 68071
- Product ID
- 68071-3241_bb14cafb-a8fa-5b6a-e053-2995a90ab47a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA087022
- Marketing category
- ANDA
- Marketing start
- 2007-12-01
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-3241-3 | 68071324103 | 30 CAPSULE in 1 BOTTLE (68071-3241-3) | 30 capsule | 2017-05-09 | 0000-00-00 | No | No | Current |