Chlorpromazine Hydrochloride
- Product NDC
- 68151-2478
- 11-digit product format
- 681512478
- Labeler code
- 68151
- Product ID
- 68151-2478_69914db1-4541-43e6-860d-5db847aad97e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine Hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA084112
- Marketing category
- ANDA
- Marketing start
- 2011-08-03
- Marketing end
- 0000-00-00
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Phenothiazines [CS],Phenothiazine [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 68151-2478-7 | Chlorpromazine Hydrochloride | 1 in 1 CUP | TABLET, SUGAR COATED | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2478 | CHLORPROMAZINE HYDROCHLORIDE TABLET, SUGAR COATED [CARILION MATERIALS MANAGEMENT] | 2 | Legacy NDC, 1 package rows | 20160229_f2f6ab54-5bab-4fa7-a7ac-0ec3bbc75bfd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2478-7 | 68151247807 | 1 in 1 CUP | Historical |