Chlorpromazine hydrochloride
- Product NDC
- 0904-7133
- 11-digit product format
- 009047133
- Labeler code
- 0904
- Product ID
- 0904-7133_efc16dbf-a0d5-4693-a2e0-d114d265f07b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorpromazine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA213368
- Marketing category
- ANDA
- Marketing start
- 2020-01-27
- Marketing end
- 0000-00-00
- Substance
- CHLORPROMAZINE HYDROCHLORIDE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0904-7133-61 | Chlorpromazine hydrochloride | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 7 |
| 0904-7133-61 | Chlorpromazine hydrochloride | 100 in 1 CARTON | TABLET, FILM COATED | 100 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-7133 | CHLORPROMAZINE HYDROCHLORIDE TABLET, FILM COATED [MAJOR PHARMACEUTICALS] | 5 | Legacy NDC, 2 package rows | 20241018_d58570a0-58b0-4662-b2ad-aa8d1463b4c1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-7133-61 | 00904713361 | 100 BLISTER PACK in 1 CARTON (0904-7133-61) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 100 blister pack | 2020-01-27 | 0000-00-00 | No | No | Current |