ACID CONTROLLER
- Product NDC
- 51316-739
- 11-digit product format
- 513160739
- Labeler code
- 51316
- Product ID
- 51316-739_c0177126-452f-4f4e-87e6-aedae9c6be1f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cimetidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
- Application
- ANDA075285
- Marketing category
- ANDA
- Marketing start
- 2026-04-08
- Substance
- CIMETIDINE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ACID CONTROLLER
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CIMETIDINE | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 80061L1WGD |
| Rxcui | 197505 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51316-739-76 | ACID CONTROLLER | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 2 |
| 51316-739-76 | ACID CONTROLLER | 120 in 1 BOTTLE | TABLET, FILM COATED | 120 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51316-739-76 | 51316073976 | 1 BOTTLE in 1 CARTON (51316-739-76) / 120 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2026-04-08 | No | No | Historical |