Citalopram
- Product NDC
- 70518-4476
- 11-digit product format
- 705184476
- Labeler code
- 70518
- Product ID
- 70518-4476_50c3aec6-ff7b-95c1-e063-6294a90ae96b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078216
- Marketing category
- ANDA
- Marketing start
- 2025-09-11
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Citalopram
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CITALOPRAM HYDROBROMIDE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | I1E9D14F36 |
| Rxcui | 283672 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4476-0 | Citalopram | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | | 3 |
| 70518-4476-1 | Citalopram | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4476-0 | 70518447600 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4476-0) | 2025-09-11 | No | No | Historical |
| 70518-4476-1 | 70518447601 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4476-1) | 2026-01-22 | No | No | Historical |