Citalopram
- Product NDC
- 52959-773
- 11-digit product format
- 529590773
- Labeler code
- 52959
- Product ID
- 52959-773_3ccdc4a4-7388-4383-964b-1e964890e1d1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- H.J. Harkins Company, Inc.
- Application
- ANDA077031
- Marketing category
- ANDA
- Marketing start
- 2009-01-01
- Marketing end
- 0000-00-00
- Substance
- CITALOPRAM HYDROBROMIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- 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 |
|---|
| 52959-773-30 | Citalopram | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 52959-773-52 | Citalopram | 52 in 1 BOTTLE | TABLET | 52 | | 1 |
| 52959-773-60 | Citalopram | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| CITALOPRAM HYDROBROMIDE | ACTIVE INGREDIENT | I1E9D14F36 | CITALOPRAM (CITALOPRAM) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| CITALOPRAM | ACTIVE MOIETY | 0DHU5B8D6V | CITALOPRAM (CITALOPRAM) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | CITALOPRAM (CITALOPRAM) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| COPOVIDONE | INACTIVE INGREDIENT | D9C330MD8B | CITALOPRAM (CITALOPRAM) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | CITALOPRAM (CITALOPRAM) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | CITALOPRAM (CITALOPRAM) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | CITALOPRAM (CITALOPRAM) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | CITALOPRAM (CITALOPRAM) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | CITALOPRAM (CITALOPRAM) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| POLYETHYLENE GLYCOL | INACTIVE INGREDIENT | 3WJQ0SDW1A | CITALOPRAM (CITALOPRAM) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | CITALOPRAM (CITALOPRAM) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | CITALOPRAM (CITALOPRAM) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52959-773 | CITALOPRAM (CITALOPRAM) TABLET [H.J. HARKINS COMPANY, INC.] | 1 | Legacy NDC, 3 package rows | 20111118_33694be4-87ce-4d25-92f6-6ae517bdf5ff.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 52959-773-30 | 52959077330 | 30 in 1 BOTTLE | Historical |
| 52959-773-52 | 52959077352 | 52 in 1 BOTTLE | Historical |
| 52959-773-60 | 52959077360 | 60 in 1 BOTTLE | Historical |