Citalopram Hydrobromide
- Product NDC
- 70518-0542
- 11-digit product format
- 705180542
- Labeler code
- 70518
- Product ID
- 70518-0542_e1e4b8f2-089b-9fee-e053-2995a90a12d1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078216
- Marketing category
- ANDA
- Marketing start
- 2017-05-17
- Marketing end
- 0000-00-00
- Substance
- CITALOPRAM HYDROBROMIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-0542 | CITALOPRAM HYDROBROMIDE TABLET [REMEDYREPACK INC.] | 17 | Legacy NDC | 20250114_6f6f01c1-a04c-4217-a1b6-6877face5375.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0542-0 | 70518054200 | 30 TABLET in 1 BLISTER PACK (70518-0542-0) | 30 tablet | 2017-05-17 | 0000-00-00 | No | No | Current |
| 70518-0542-1 | 70518054201 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-0542-1) | 90 tablet | 2019-04-25 | 0000-00-00 | No | No | Current |