Diethylpropion HCl Controlled-Release
- Product NDC
- 21695-876
- 11-digit product format
- 216950876
- Labeler code
- 21695
- Product ID
- 21695-876_f30aa4fe-15ac-4412-afae-fae3b940a74c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diethylpropion hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- NDA011722
- Marketing category
- NDA
- Marketing start
- 2008-01-01
- Marketing end
- 0000-00-00
- Substance
- DIETHYLPROPION HYDROCHLORIDE
- Active strength
- 75 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21695-876-30 | Diethylpropion HCl Controlled-Release | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-876 | DIETHYLPROPION HCL CONTROLLED-RELEASE (DIETHYLPROPION HYDROCHLORIDE) TABLET [REBEL DISTRIBUTORS CORP] | 2 | Legacy NDC, 1 package rows | 20110224_b26c2f51-7436-4622-a174-3f3978a1fda2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-876-30 | 21695087630 | 30 in 1 BOTTLE | Historical |